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CHROM
POS
REF
ALT
Gene
HGVS.c
HGVS.p
dbSNP142 ID
chr19
38959680
C
T
synonymous_variant
LOW
RYR1
c.3456C>T
chr19
38956839
C
T
synonymous_variant
LOW
RYR1
c.2979C>T
chr19
38956803
G
A
synonymous_variant
LOW
RYR1
c.2943G>A
chr19
38953996
A
G
intron_variant
MODIFIER
RYR1
c.2578-67A>G
chr19
38950947
C
T
intron_variant
MODIFIER
RYR1
c.2361-68C>T
chr19
38949904
C
T
synonymous_variant
LOW
RYR1
c.2286C>T
chr19
38949729
T
G
intron_variant
MODIFIER
RYR1
c.2168-57T>G
chr19
38948963
C
G
intron_variant
MODIFIER
RYR1
c.2167+31C>G
chr19
38948356
T
C
intron_variant
MODIFIER
RYR1
c.1925+86T>C
chr19
38946215
G
C
intron_variant
MODIFIER
RYR1
c.1672+29G>C
chr19
38946182
G
A
synonymous_variant
LOW
RYR1
c.1668G>A
chr19
38945851
T
C
intron_variant
MODIFIER
RYR1
c.1441-24T>C
chr19
38943728
G
A
intron_variant
MODIFIER
RYR1
c.1440+74G>A
chr19
38939505
T
C
intron_variant
MODIFIER
RYR1
c.1122+52T>C
chr19
38939408
T
C
synonymous_variant
LOW
RYR1
c.1077T>C
chr19
38935350
T
TC
intron_variant
MODIFIER
RYR1
c.631+33_631+34insC
chr19
38935280
A
G
synonymous_variant
LOW
RYR1
c.594A>G
chr19
38931578
G
C
intron_variant
MODIFIER
RYR1
c.165+74G>C
chr19
38924814
T
C
intron_variant
MODIFIER
RYR1
c.45+300T>C
chr19
18990982
C
T
intron_variant
MODIFIER
GDF1
c.-571+101G>A