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rs370069461

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs370069461(C;T)
Make rs370069461(T;T)
ReferenceGRCh38.p2 38.2/147
Chromosome14
Position23417669
GeneMHRT, MIR208B, MYH7
is asnp
is mentioned by
dbSNPrs370069461
ebirs370069461
HLIrs370069461
Exacrs370069461
Varsomers370069461
Maprs370069461
PheGenIrs370069461
hapmaprs370069461
1000 genomesrs370069461
hgdprs370069461
ensemblrs370069461
gopubmedrs370069461
geneviewrs370069461
scholarrs370069461
googlers370069461
pharmgkbrs370069461
gwascentralrs370069461
openSNPrs370069461
23andMers370069461
23andMe allrs370069461
SNP Nexus

SNPshotrs370069461
SNPdbers370069461
MSV3drs370069461
GWAS Ctlgrs370069461
Max Magnitude0
ClinVar
Risk rs370069461(T;T)
Alt rs370069461(T;T)
Reference rs370069461(C;C)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene MYH7 MIR208B MHRT
CLNDBN not provided
Reversed 0
HGVS NC_000014.8:g.23886878C>T
CLNSRC
CLNACC RCV000158641.2,