rs145983824

Orientation

plus

Stabilized

plus

Geno	Mag	Summary
(C;C)	0	common in clinvar

Make rs145983824(C;T)

Make rs145983824(T;T)

Reference

GRCh38.p2 38.2/144

Chromosome

10

Position

86718110

Gene

LDB3

is a	snp
is	mentioned by
dbSNP	rs145983824
dbSNP (classic)	rs145983824
ClinGen	rs145983824
ebi	rs145983824
HLI	rs145983824
Exac	rs145983824
Gnomad	rs145983824
Varsome	rs145983824
LitVar	rs145983824
Map	rs145983824
PheGenI	rs145983824
Biobank	rs145983824
1000 genomes	rs145983824
hgdp	rs145983824
ensembl	rs145983824
geneview	rs145983824
scholar	rs145983824
google	rs145983824
pharmgkb	rs145983824
gwascentral	rs145983824
openSNP	rs145983824
23andMe	rs145983824
SNPshot	rs145983824
SNPdbe	rs145983824
MSV3d	rs145983824
GWAS Ctlg	rs145983824

Max Magnitude

0

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	RCV000038742.3, RCV000170304.3,