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rs775636212

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs775636212(C;T)
Make rs775636212(T;T)
ReferenceGRCh38.p2 38.2/144
Chromosome17
Position39665813
GeneTCAP
is asnp
is mentioned by
dbSNPrs775636212
ebirs775636212
HLIrs775636212
Exacrs775636212
Varsomers775636212
Maprs775636212
PheGenIrs775636212
hapmaprs775636212
1000 genomesrs775636212
hgdprs775636212
ensemblrs775636212
gopubmedrs775636212
geneviewrs775636212
scholarrs775636212
googlers775636212
pharmgkbrs775636212
gwascentralrs775636212
openSNPrs775636212
23andMers775636212
23andMe allrs775636212
SNP Nexus

SNPshotrs775636212
SNPdbers775636212
MSV3drs775636212
GWAS Ctlgrs775636212
Max Magnitude0
ClinVar
Risk rs775636212(T;T)
Alt rs775636212(T;T)
Reference rs775636212(C;C)
Significance Pathogenic
Disease Dilated cardiomyopathy 1N Hypertrophic cardiomyopathy
Variation info
Gene TCAP
CLNDBN Dilated cardiomyopathy 1N Hypertrophic cardiomyopathy
Reversed 0
HGVS NC_000017.10:g.37822066C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000170303.4, RCV000172108.2,