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rs397516162

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs397516162(C;G)
Make rs397516162(G;G)
ReferenceGRCh38.p2 38.2/144
Chromosome14
Position23424146
GeneMYH7
is asnp
is mentioned by
dbSNPrs397516162
ebirs397516162
HLIrs397516162
Exacrs397516162
Varsomers397516162
Maprs397516162
PheGenIrs397516162
hapmaprs397516162
1000 genomesrs397516162
hgdprs397516162
ensemblrs397516162
gopubmedrs397516162
geneviewrs397516162
scholarrs397516162
googlers397516162
pharmgkbrs397516162
gwascentralrs397516162
openSNPrs397516162
23andMers397516162
23andMe allrs397516162
SNP Nexus

SNPshotrs397516162
SNPdbers397516162
MSV3drs397516162
GWAS Ctlgrs397516162
Max Magnitude0
ClinVar
Risk rs397516162(A,G;A,G)
Alt rs397516162(A,G;A,G)
Reference rs397516162(C;C)
Significance Probable-Pathogenic
Disease not specified
Variation info
Gene MYH7
CLNDBN not specified
Reversed 1
HGVS NC_000014.8:g.23893355G>C; NC_000014.8:g.23893355G>T
CLNSRC
CLNACC RCV000035813.3, RCV000168877.2,