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rs397516088

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs397516088(A;A)
Make rs397516088(A;G)
ReferenceGRCh38.p2 38.2/144
Chromosome14
Position23429850
GeneMYH7
is asnp
is mentioned by
dbSNPrs397516088
ebirs397516088
HLIrs397516088
Exacrs397516088
Varsomers397516088
Maprs397516088
PheGenIrs397516088
hapmaprs397516088
1000 genomesrs397516088
hgdprs397516088
ensemblrs397516088
gopubmedrs397516088
geneviewrs397516088
scholarrs397516088
googlers397516088
pharmgkbrs397516088
gwascentralrs397516088
openSNPrs397516088
23andMers397516088
23andMe allrs397516088
SNP Nexus

SNPshotrs397516088
SNPdbers397516088
MSV3drs397516088
GWAS Ctlgrs397516088
Max Magnitude0
ClinVar
Risk rs397516088(A;A)
Alt rs397516088(A;A)
Reference rs397516088(G;G)
Significance Probable-Pathogenic
Disease not specified not provided
Variation info
Gene MYH7
CLNDBN not specified not provided
Reversed 1
HGVS NC_000014.8:g.23899059C>T
CLNSRC
CLNACC RCV000035696.2, RCV000225736.1,