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rs377461670

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs377461670(A;A)
Make rs377461670(A;G)
ReferenceGRCh38.p2 38.2/144
Chromosome14
Position23415757
GeneMHRT, MYH7
is asnp
is mentioned by
dbSNPrs377461670
ebirs377461670
HLIrs377461670
Exacrs377461670
Varsomers377461670
Maprs377461670
PheGenIrs377461670
hapmaprs377461670
1000 genomesrs377461670
hgdprs377461670
ensemblrs377461670
gopubmedrs377461670
geneviewrs377461670
scholarrs377461670
googlers377461670
pharmgkbrs377461670
gwascentralrs377461670
openSNPrs377461670
23andMers377461670
23andMe allrs377461670
SNP Nexus

SNPshotrs377461670
SNPdbers377461670
MSV3drs377461670
GWAS Ctlgrs377461670
Max Magnitude0
ClinVar
Risk rs377461670(A;A)
Alt rs377461670(A;A)
Reference rs377461670(G;G)
Significance Pathogenic
Disease not specified
Variation info
Gene MYH7 MHRT
CLNDBN not specified
Reversed 0
HGVS NC_000014.8:g.23884966G>A
CLNSRC
CLNACC RCV000158681.2,