rs786205624

Orientation

minus

Stabilized

minus

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

Make rs786205624(C;C)

Make rs786205624(C;G)

Reference

GRCh38.p2 38.2/146

Chromosome

14

Position

74526070

Gene

LTBP2

is a	snp
is	mentioned by
dbSNP	rs786205624
dbSNP (classic)	rs786205624
ClinGen	rs786205624
ebi	rs786205624
HLI	rs786205624
Exac	rs786205624
Gnomad	rs786205624
Varsome	rs786205624
LitVar	rs786205624
Map	rs786205624
PheGenI	rs786205624
Biobank	rs786205624
1000 genomes	rs786205624
hgdp	rs786205624
ensembl	rs786205624
geneview	rs786205624
scholar	rs786205624
google	rs786205624
pharmgkb	rs786205624
gwascentral	rs786205624
openSNP	rs786205624
23andMe	rs786205624
SNPshot	rs786205624
SNPdbe	rs786205624
MSV3d	rs786205624
GWAS Ctlg	rs786205624

Max Magnitude

0

ClinVar
Risk	rs786205624(C;C) rs786205624(T;T)
Alt	rs786205624(C;C) rs786205624(T;T)
Reference	Rs786205624(G;G)
Significance	Probable-Pathogenic
Disease	not provided
Variation	info
Gene	LTBP2
CLNDBN	not provided
Reversed	1
HGVS	NC_000014.8:g.74992773C>G
CLNSRC
CLNACC	RCV000171477.1,