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rs145983824

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs145983824(C;T)
Make rs145983824(T;T)
ReferenceGRCh38.p2 38.2/144
Chromosome10
Position86718110
GeneLDB3
is asnp
is mentioned by
dbSNPrs145983824
ebirs145983824
HLIrs145983824
Exacrs145983824
Varsomers145983824
Maprs145983824
PheGenIrs145983824
hapmaprs145983824
1000 genomesrs145983824
hgdprs145983824
ensemblrs145983824
gopubmedrs145983824
geneviewrs145983824
scholarrs145983824
googlers145983824
pharmgkbrs145983824
gwascentralrs145983824
openSNPrs145983824
23andMers145983824
23andMe allrs145983824
SNP Nexus

SNPshotrs145983824
SNPdbers145983824
MSV3drs145983824
GWAS Ctlgrs145983824
Max Magnitude0
ClinVar
Risk rs145983824(T;T)
Alt rs145983824(T;T)
Reference rs145983824(C;C)
Significance Pathogenic
Disease not specified Familial hypertrophic cardiomyopathy 24
Variation info
Gene LDB3
CLNDBN not specified Familial hypertrophic cardiomyopathy 24
Reversed 0
HGVS NC_000010.10:g.88477867C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000038742.2, RCV000170304.3,