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CHROM
POS
REF
ALT
Gene
HGVS.c
HGVS.p
dbSNP142 ID
chr2
175614908
CAAA
C
intron_variant
MODIFIER
CHRNA1
c.854-14_854-12delTTT
chr2
175613600
T
C
intron_variant
MODIFIER
CHRNA1
c.1078-53A>G
chr2
175613059
A
C
intron_variant
MODIFIER
CHRNA1
c.1318-76T>G
chr2
170218847
C
G
synonymous_variant
LOW
LRP2
c.63G>C
chr2
170218816
T
C
intron_variant
MODIFIER
LRP2
c.79+15A>G
chr2
170177382
G
A
missense_variant
MODERATE
LRP2
c.92C>T
chr2
170150671
G
A
synonymous_variant
LOW
LRP2
c.639C>T
chr2
170139346
C
T
intron_variant
MODIFIER
LRP2
c.1171+37G>A
chr2
170134191
G
C
intron_variant
MODIFIER
LRP2
c.1772+64C>G
chr2
170129636
A
G
intron_variant
MODIFIER
LRP2
c.1976-59T>C
chr2
170129528
G
A
synonymous_variant
LOW
LRP2
c.2025C>T
chr2
170115588
T
C
synonymous_variant
LOW
LRP2
c.2460A>G
chr2
170103351
G
T
synonymous_variant
LOW
LRP2
c.3054C>A
chr2
170103336
T
C
synonymous_variant
LOW
LRP2
c.3069A>G
chr2
170099899
G
A
intron_variant
MODIFIER
LRP2
c.3550+14C>T
chr2
170099895
A
C
intron_variant
MODIFIER
LRP2
c.3550+18T>G
chr2
170099473
T
C
synonymous_variant
LOW
LRP2
c.3660A>G
chr2
170099446
T
G
intron_variant
MODIFIER
LRP2
c.3667+20A>C
chr2
170096018
G
A
intron_variant
MODIFIER
LRP2
c.4294+19C>T
chr2
170092395
A
G
synonymous_variant
LOW
LRP2
c.4875T>C