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rs199476416

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs199476416(C;C)
Make rs199476416(C;G)
ReferenceGRCh38.p2 38.2/146
Chromosome10
Position68206903
GeneLOC105378341, MYPN
is asnp
is mentioned by
dbSNPrs199476416
ebirs199476416
HLIrs199476416
Exacrs199476416
Varsomers199476416
Maprs199476416
PheGenIrs199476416
hapmaprs199476416
1000 genomesrs199476416
hgdprs199476416
ensemblrs199476416
gopubmedrs199476416
geneviewrs199476416
scholarrs199476416
googlers199476416
pharmgkbrs199476416
gwascentralrs199476416
openSNPrs199476416
23andMers199476416
23andMe allrs199476416
SNP Nexus

SNPshotrs199476416
SNPdbers199476416
MSV3drs199476416
GWAS Ctlgrs199476416
Max Magnitude0
ClinVar
Risk rs199476416(A,C;A,C)
Alt rs199476416(A,C;A,C)
Reference rs199476416(G;G)
Significance Probable-Pathogenic
Disease not provided Dilated cardiomyopathy 1KK
Variation info
Gene MYPN
CLNDBN not provided Dilated cardiomyopathy 1KK
Reversed 0
HGVS NC_000010.10:g.69966660G>A; NC_000010.10:g.69966660G>C
CLNSRC Leiden Muscular Dystrophy pages (MYPN)
CLNACC RCV000183599.2, RCV000024507.1, RCV000207010.1,