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rs771297865

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs771297865(C;T)
Make rs771297865(T;T)
ReferenceGRCh38.p2 38.2/147
Chromosome16
Position15737617
GeneMYH11
is asnp
is mentioned by
dbSNPrs771297865
ebirs771297865
HLIrs771297865
Exacrs771297865
Varsomers771297865
Maprs771297865
PheGenIrs771297865
hapmaprs771297865
1000 genomesrs771297865
hgdprs771297865
ensemblrs771297865
gopubmedrs771297865
geneviewrs771297865
scholarrs771297865
googlers771297865
pharmgkbrs771297865
gwascentralrs771297865
openSNPrs771297865
23andMers771297865
23andMe allrs771297865
SNP Nexus

SNPshotrs771297865
SNPdbers771297865
MSV3drs771297865
GWAS Ctlgrs771297865
Max Magnitude0
ClinVar
Risk rs771297865(T;T)
Alt rs771297865(T;T)
Reference rs771297865(C;C)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene MYH11
CLNDBN not provided
Reversed 0
HGVS NC_000016.9:g.15831474C>T
CLNSRC
CLNACC RCV000182502.2,