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rs149840927

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs149840927(G;T)
Make rs149840927(T;T)
ReferenceGRCh38.p2 38.2/144
Chromosome14
Position23423672
GeneMYH7
is asnp
is mentioned by
dbSNPrs149840927
ebirs149840927
HLIrs149840927
Exacrs149840927
Varsomers149840927
Maprs149840927
PheGenIrs149840927
hapmaprs149840927
1000 genomesrs149840927
hgdprs149840927
ensemblrs149840927
gopubmedrs149840927
geneviewrs149840927
scholarrs149840927
googlers149840927
pharmgkbrs149840927
gwascentralrs149840927
openSNPrs149840927
23andMers149840927
23andMe allrs149840927
SNP Nexus

SNPshotrs149840927
SNPdbers149840927
MSV3drs149840927
GWAS Ctlgrs149840927
Max Magnitude0
ClinVar
Risk rs149840927(T;T)
Alt rs149840927(T;T)
Reference rs149840927(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene MYH7
CLNDBN not provided
Reversed 0
HGVS NC_000014.8:g.23892881G>T
CLNSRC
CLNACC RCV000158581.2,