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CHROM
POS
REF
ALT
Gene
HGVS.c
HGVS.p
dbSNP142 ID
chr2
170089851
G
A
intron_variant
MODIFIER
LRP2
c.5098+70C>T
chr2
170089824
T
C
intron_variant
MODIFIER
LRP2
c.5098+97A>G
chr2
170088506
T
C
intron_variant
MODIFIER
LRP2
c.5099-154A>G
chr2
170088477
T
C
intron_variant
MODIFIER
LRP2
c.5099-125A>G
chr2
170082013
A
G
intron_variant
MODIFIER
LRP2
c.5395-50T>C
chr2
170077165
C
T
intron_variant
MODIFIER
LRP2
c.5539-92G>A
chr2
170063783
T
C
intron_variant
MODIFIER
LRP2
c.6470-23A>G
chr2
170059190
T
C
intron_variant
MODIFIER
LRP2
c.8209+76A>G
chr2
170055255
T
C
intron_variant
MODIFIER
LRP2
c.8578+41A>G
chr2
170053580
C
T
intron_variant
MODIFIER
LRP2
c.8579-40G>A
chr2
170053505
C
T
missense_variant
MODERATE
LRP2
c.8614G>A
chr2
170050472
T
C
intron_variant
MODIFIER
LRP2
c.8699-70A>G
chr2
170031824
C
T
synonymous_variant
LOW
LRP2
c.10647G>A
chr2
167168093
C
T
synonymous_variant
LOW
SCN9A
c.174G>A
chr2
167163373
C
A
intron_variant
MODIFIER
SCN9A
c.377+93G>T
chr2
167163372
T
C
intron_variant
MODIFIER
SCN9A
c.377+94A>G
chr2
167163199
A
T
intron_variant
MODIFIER
SCN9A
c.378-90T>A
chr2
167163043
T
C
synonymous_variant
LOW
SCN9A
c.444A>G
chr2
167162277
G
A
intron_variant
MODIFIER
SCN9A
c.596+25C>T
chr2
167145142
A
G
synonymous_variant
LOW
SCN9A
c.1119T>C