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rs730880800

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs730880800(C;T)
Make rs730880800(T;T)
ReferenceGRCh38.p2 38.2/144
Chromosome14
Position23417556
GeneMHRT, MIR208B, MYH7
is asnp
is mentioned by
dbSNPrs730880800
ebirs730880800
HLIrs730880800
Exacrs730880800
Varsomers730880800
Maprs730880800
PheGenIrs730880800
hapmaprs730880800
1000 genomesrs730880800
hgdprs730880800
ensemblrs730880800
gopubmedrs730880800
geneviewrs730880800
scholarrs730880800
googlers730880800
pharmgkbrs730880800
gwascentralrs730880800
openSNPrs730880800
23andMers730880800
23andMe allrs730880800
SNP Nexus

SNPshotrs730880800
SNPdbers730880800
MSV3drs730880800
GWAS Ctlgrs730880800
Max Magnitude0
ClinVar
Risk rs730880800(T;T)
Alt rs730880800(T;T)
Reference rs730880800(C;C)
Significance Pathogenic
Disease not specified
Variation info
Gene MYH7 MIR208B MHRT
CLNDBN not specified
Reversed 1
HGVS NC_000014.8:g.23886765G>A
CLNSRC
CLNACC RCV000158653.2,