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rs397516214

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs397516214(C;G)
Make rs397516214(G;G)
ReferenceGRCh38.p2 38.2/144
Chromosome14
Position23417273
GeneMHRT, MYH7
is asnp
is mentioned by
dbSNPrs397516214
ebirs397516214
HLIrs397516214
Exacrs397516214
Varsomers397516214
Maprs397516214
PheGenIrs397516214
hapmaprs397516214
1000 genomesrs397516214
hgdprs397516214
ensemblrs397516214
gopubmedrs397516214
geneviewrs397516214
scholarrs397516214
googlers397516214
pharmgkbrs397516214
gwascentralrs397516214
openSNPrs397516214
23andMers397516214
23andMe allrs397516214
SNP Nexus

SNPshotrs397516214
SNPdbers397516214
MSV3drs397516214
GWAS Ctlgrs397516214
Max Magnitude0
ClinVar
Risk rs397516214(G;G)
Alt rs397516214(G;G)
Reference rs397516214(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.23886482G>C
CLNSRC
CLNACC RCV000035909.3, RCV000158865.1,