Have questions? Visit https://www.reddit.com/r/SNPedia

rs397516175

From SNPedia

Orientationminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs397516175(A;T)
Make rs397516175(T;T)
ReferenceGRCh38.p2 38.2/144
Chromosome14
Position23423983
GeneMYH7
is asnp
is mentioned by
dbSNPrs397516175
ebirs397516175
HLIrs397516175
Exacrs397516175
Varsomers397516175
Maprs397516175
PheGenIrs397516175
hapmaprs397516175
1000 genomesrs397516175
hgdprs397516175
ensemblrs397516175
gopubmedrs397516175
geneviewrs397516175
scholarrs397516175
googlers397516175
pharmgkbrs397516175
gwascentralrs397516175
openSNPrs397516175
23andMers397516175
23andMe allrs397516175
SNP Nexus

SNPshotrs397516175
SNPdbers397516175
MSV3drs397516175
GWAS Ctlgrs397516175
Max Magnitude0
ClinVar
Risk rs397516175(T;T)
Alt rs397516175(T;T)
Reference rs397516175(A;A)
Significance Probable-Pathogenic
Disease not specified not provided
Variation info
Gene MYH7
CLNDBN not specified not provided
Reversed 1
HGVS NC_000014.8:g.23893192T>A
CLNSRC
CLNACC RCV000035830.2, RCV000158578.2,