Have questions? Visit https://www.reddit.com/r/SNPedia

rs149887823

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs149887823(C;T)
Make rs149887823(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome10
Position68189064
GeneMYPN
is asnp
is mentioned by
dbSNPrs149887823
dbSNP (old)rs149887823
ClinGenrs149887823
ebirs149887823
HLIrs149887823
Exacrs149887823
Gnomadrs149887823
Varsomers149887823
Maprs149887823
PheGenIrs149887823
Biobankrs149887823
1000 genomesrs149887823
hgdprs149887823
ensemblrs149887823
gopubmedrs149887823
geneviewrs149887823
scholarrs149887823
googlers149887823
pharmgkbrs149887823
gwascentralrs149887823
openSNPrs149887823
23andMers149887823
23andMe allrs149887823
SNP Nexus

SNPshotrs149887823
SNPdbers149887823
MSV3drs149887823
GWAS Ctlgrs149887823
Max Magnitude0
ClinVar
Risk rs149887823(G;G) rs149887823(T;T)
Alt rs149887823(G;G) rs149887823(T;T)
Reference Rs149887823(C;C)
Significance Probable-non-pathogenic
Disease not provided Dilated cardiomyopathy 1KK not specified
Variation info
Gene MYPN
CLNDBN not provided Dilated cardiomyopathy 1KK not specified
Reversed 0
HGVS NC_000010.10:g.69948821C>T
CLNSRC UniProtKB (protein)
CLNACC RCV000172574.1, RCV000207001.1, RCV000221588.3,