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rs201082272

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs201082272(C;G)
Make rs201082272(G;G)
ReferenceGRCh38.p7 38.3/150
Chromosome17
Position10535366
GeneMYHAS, MYH2
is asnp
is mentioned by
dbSNPrs201082272
dbSNP (old)rs201082272
ClinGenrs201082272
ebirs201082272
HLIrs201082272
Exacrs201082272
Gnomadrs201082272
Varsomers201082272
Maprs201082272
PheGenIrs201082272
Biobankrs201082272
1000 genomesrs201082272
hgdprs201082272
ensemblrs201082272
gopubmedrs201082272
geneviewrs201082272
scholarrs201082272
googlers201082272
pharmgkbrs201082272
gwascentralrs201082272
openSNPrs201082272
23andMers201082272
23andMe allrs201082272
SNPshotrs201082272
SNPdbers201082272
MSV3drs201082272
GWAS Ctlgrs201082272
Max Magnitude0
ClinVar
Risk rs201082272(G;G) rs201082272(T;T)
Alt rs201082272(G;G) rs201082272(T;T)
Reference Rs201082272(C;C)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene MYH2 MYHAS
CLNDBN not provided
Reversed 0
HGVS NC_000017.10:g.10438683C>G
CLNSRC
CLNACC RCV000413648.1,