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rs201675951

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs201675951(A;A)
Make rs201675951(A;G)
ReferenceGRCh38 38.1/142
Chromosome1
Position237610770
GeneRYR2
is asnp
is mentioned by
dbSNPrs201675951
ebirs201675951
HLIrs201675951
Exacrs201675951
Varsomers201675951
Maprs201675951
PheGenIrs201675951
hapmaprs201675951
1000 genomesrs201675951
hgdprs201675951
ensemblrs201675951
gopubmedrs201675951
geneviewrs201675951
scholarrs201675951
googlers201675951
pharmgkbrs201675951
gwascentralrs201675951
openSNPrs201675951
23andMers201675951
23andMe allrs201675951
SNP Nexus

SNPshotrs201675951
SNPdbers201675951
MSV3drs201675951
GWAS Ctlgrs201675951
Max Magnitude0
ClinVar
Risk rs201675951(A;A)
Alt rs201675951(A;A)
Reference rs201675951(G;G)
Significance Probable-Pathogenic
Disease Primary dilated cardiomyopathy Primary familial hypertrophic cardiomyopathy not specified
Variation info
Gene RYR2
CLNDBN Primary dilated cardiomyopathy Primary familial hypertrophic cardiomyopathy not specified
Reversed 0
HGVS NC_000001.10:g.237774070G>A
CLNSRC ClinVar
CLNACC RCV000143946.2, RCV000157455.1, RCV000182725.2,