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rs397516231

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs397516231(C;T)
Make rs397516231(T;T)
ReferenceGRCh38.p2 38.2/144
Chromosome14
Position23416093
GeneMHRT, MYH7
is asnp
is mentioned by
dbSNPrs397516231
ebirs397516231
HLIrs397516231
Exacrs397516231
Varsomers397516231
Maprs397516231
PheGenIrs397516231
hapmaprs397516231
1000 genomesrs397516231
hgdprs397516231
ensemblrs397516231
gopubmedrs397516231
geneviewrs397516231
scholarrs397516231
googlers397516231
pharmgkbrs397516231
gwascentralrs397516231
openSNPrs397516231
23andMers397516231
23andMe allrs397516231
SNP Nexus

SNPshotrs397516231
SNPdbers397516231
MSV3drs397516231
GWAS Ctlgrs397516231
Max Magnitude0
ClinVar
Risk rs397516231(T;T)
Alt rs397516231(T;T)
Reference rs397516231(C;C)
Significance Probable-Pathogenic
Disease not specified not provided
Variation info
Gene MYH7 MHRT
CLNDBN not specified not provided
Reversed 1
HGVS NC_000014.8:g.23885302G>A
CLNSRC
CLNACC RCV000035936.3, RCV000158675.1,