rs200639270

Orientation

plus

Stabilized

plus

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

Make rs200639270(A;A)

Make rs200639270(A;G)

Reference

GRCh38.p7 38.3/150

Chromosome

19

Position

12893543

Gene

GCDH

is a	snp
is	mentioned by
dbSNP	rs200639270
dbSNP (classic)	rs200639270
ClinGen	rs200639270
ebi	rs200639270
HLI	rs200639270
Exac	rs200639270
Gnomad	rs200639270
Varsome	rs200639270
LitVar	rs200639270
Map	rs200639270
PheGenI	rs200639270
Biobank	rs200639270
1000 genomes	rs200639270
hgdp	rs200639270
ensembl	rs200639270
geneview	rs200639270
scholar	rs200639270
google	rs200639270
pharmgkb	rs200639270
gwascentral	rs200639270
openSNP	rs200639270
23andMe	rs200639270
SNPshot	rs200639270
SNPdbe	rs200639270
MSV3d	rs200639270
GWAS Ctlg	rs200639270

Max Magnitude

0

ClinVar
Risk	rs200639270(A;A)
Alt	rs200639270(A;A)
Reference	Rs200639270(G;G)
Significance	Pathogenic
Disease	not provided
Variation	info
Gene	GCDH
CLNDBN	not provided
Reversed	0
HGVS	NC_000019.9:g.13004357G>A
CLNSRC
CLNACC	RCV000444441.1,