rs786205577

Orientation

plus

Stabilized

plus

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

Make rs786205577(A;G)

Make rs786205577(G;G)

Reference

GRCh38.p2 38.2/146

Chromosome

6

Position

10626423

Gene

GCNT2

is a	snp
is	mentioned by
dbSNP	rs786205577
dbSNP (classic)	rs786205577
ClinGen	rs786205577
ebi	rs786205577
HLI	rs786205577
Exac	rs786205577
Gnomad	rs786205577
Varsome	rs786205577
LitVar	rs786205577
Map	rs786205577
PheGenI	rs786205577
Biobank	rs786205577
1000 genomes	rs786205577
hgdp	rs786205577
ensembl	rs786205577
geneview	rs786205577
scholar	rs786205577
google	rs786205577
pharmgkb	rs786205577
gwascentral	rs786205577
openSNP	rs786205577
23andMe	rs786205577
SNPshot	rs786205577
SNPdbe	rs786205577
MSV3d	rs786205577
GWAS Ctlg	rs786205577

Max Magnitude

0

ClinVar
Risk	rs786205577(G;G)
Alt	rs786205577(G;G)
Reference	Rs786205577(A;A)
Significance	Probable-Pathogenic
Disease	not provided
Variation	info
Gene	GCNT2
CLNDBN	not provided
Reversed	0
HGVS	NC_000006.11:g.10626656A>G
CLNSRC
CLNACC	RCV000171391.1,