rs786205496

Orientation

plus

Stabilized

plus

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

Make rs786205496(A;A)

Make rs786205496(A;G)

Reference

GRCh38.p2 38.2/146

Chromosome

16

Position

8768866

Gene

ABAT

is a	snp
is	mentioned by
dbSNP	rs786205496
dbSNP (classic)	rs786205496
ClinGen	rs786205496
ebi	rs786205496
HLI	rs786205496
Exac	rs786205496
Gnomad	rs786205496
Varsome	rs786205496
LitVar	rs786205496
Map	rs786205496
PheGenI	rs786205496
Biobank	rs786205496
1000 genomes	rs786205496
hgdp	rs786205496
ensembl	rs786205496
geneview	rs786205496
scholar	rs786205496
google	rs786205496
pharmgkb	rs786205496
gwascentral	rs786205496
openSNP	rs786205496
23andMe	rs786205496
SNPshot	rs786205496
SNPdbe	rs786205496
MSV3d	rs786205496
GWAS Ctlg	rs786205496

Max Magnitude

0

ClinVar
Risk	rs786205496(A;A)
Alt	rs786205496(A;A)
Reference	Rs786205496(G;G)
Significance	Probable-Pathogenic
Disease	not provided
Variation	info
Gene	ABAT
CLNDBN	not provided
Reversed	0
HGVS	NC_000016.9:g.8862723G>A
CLNSRC
CLNACC	RCV000171244.1,