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rs773998062

From SNPedia

Orientationplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs773998062(A;G)
Make rs773998062(G;G)
ReferenceGRCh38.p2 38.2/147
Chromosome16
Position15760586
GeneMYH11
is asnp
is mentioned by
dbSNPrs773998062
ebirs773998062
HLIrs773998062
Exacrs773998062
Varsomers773998062
Maprs773998062
PheGenIrs773998062
hapmaprs773998062
1000 genomesrs773998062
hgdprs773998062
ensemblrs773998062
gopubmedrs773998062
geneviewrs773998062
scholarrs773998062
googlers773998062
pharmgkbrs773998062
gwascentralrs773998062
openSNPrs773998062
23andMers773998062
23andMe allrs773998062
SNP Nexus

SNPshotrs773998062
SNPdbers773998062
MSV3drs773998062
GWAS Ctlgrs773998062
Max Magnitude0
ClinVar
Risk rs773998062(G,T;G,T)
Alt rs773998062(G,T;G,T)
Reference rs773998062(A;A)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene MYH11
CLNDBN not provided
Reversed 0
HGVS NC_000016.9:g.15854443A>G
CLNSRC
CLNACC RCV000182553.2,