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rs876661179

From SNPedia

Orientationminus
Geno Mag Summary
(GAC;GAC) 0 common in clinvar
Make rs876661179(-;-)
Make rs876661179(-;GAC)
ReferenceGRCh38.p2 38.2/147
Chromosome14
Position23415188
GeneMHRT, MYH7
is asnp
is mentioned by
dbSNPrs876661179
ebirs876661179
HLIrs876661179
Exacrs876661179
Varsomers876661179
Maprs876661179
PheGenIrs876661179
hapmaprs876661179
1000 genomesrs876661179
hgdprs876661179
ensemblrs876661179
gopubmedrs876661179
geneviewrs876661179
scholarrs876661179
googlers876661179
pharmgkbrs876661179
gwascentralrs876661179
openSNPrs876661179
23andMers876661179
23andMe allrs876661179
SNP Nexus

SNPshotrs876661179
SNPdbers876661179
MSV3drs876661179
GWAS Ctlgrs876661179
Max Magnitude0
ClinVar
Risk rs876661179(;)
Alt rs876661179(;)
Reference rs876661179(GAC;GAC)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene MYH7 MHRT
CLNDBN not provided
Reversed 1
HGVS NC_000014.8:g.23884397_23884399delGTC
CLNSRC
CLNACC RCV000219460.1,