rs761765983

Orientation

plus

Stabilized

plus

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

Make rs761765983(A;A)

Make rs761765983(A;G)

Reference

GRCh38.p7 38.3/150

Chromosome

19

Position

12896949

Gene

GCDH

is a	snp
is	mentioned by
dbSNP	rs761765983
dbSNP (classic)	rs761765983
ClinGen	rs761765983
ebi	rs761765983
HLI	rs761765983
Exac	rs761765983
Gnomad	rs761765983
Varsome	rs761765983
LitVar	rs761765983
Map	rs761765983
PheGenI	rs761765983
Biobank	rs761765983
1000 genomes	rs761765983
hgdp	rs761765983
ensembl	rs761765983
geneview	rs761765983
scholar	rs761765983
google	rs761765983
pharmgkb	rs761765983
gwascentral	rs761765983
openSNP	rs761765983
23andMe	rs761765983
SNPshot	rs761765983
SNPdbe	rs761765983
MSV3d	rs761765983
GWAS Ctlg	rs761765983

Max Magnitude

0

ClinVar
Risk	rs761765983(A;A)
Alt	rs761765983(A;A)
Reference	Rs761765983(G;G)
Significance	Pathogenic
Disease	not provided
Variation	info
Gene	GCDH
CLNDBN	not provided
Reversed	0
HGVS	NC_000019.9:g.13007763G>A
CLNSRC
CLNACC	RCV000494627.1,