rs768526453

Orientation

plus

Stabilized

plus

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

Make rs768526453(A;A)

Make rs768526453(A;G)

Reference

GRCh38.p7 38.3/149

Chromosome

9

Position

101362924

Gene

BAAT

is a	snp
is	mentioned by
dbSNP	rs768526453
dbSNP (classic)	rs768526453
ClinGen	rs768526453
ebi	rs768526453
HLI	rs768526453
Exac	rs768526453
Gnomad	rs768526453
Varsome	rs768526453
LitVar	rs768526453
Map	rs768526453
PheGenI	rs768526453
Biobank	rs768526453
1000 genomes	rs768526453
hgdp	rs768526453
ensembl	rs768526453
geneview	rs768526453
scholar	rs768526453
google	rs768526453
pharmgkb	rs768526453
gwascentral	rs768526453
openSNP	rs768526453
23andMe	rs768526453
SNPshot	rs768526453
SNPdbe	rs768526453
MSV3d	rs768526453
GWAS Ctlg	rs768526453

Max Magnitude

0

ClinVar
Risk	rs768526453(A;A)
Alt	rs768526453(A;A)
Reference	Rs768526453(G;G)
Significance	Probable-Pathogenic
Disease	not provided not specified Hypercholanemia
Variation	info
Gene	BAAT
CLNDBN	not provided not specified Hypercholanemia
Reversed	0
HGVS	NC_000009.11:g.104125206G>A
CLNSRC	Illumina
CLNACC	RCV000171425.3, RCV000259160.1, RCV000333195.1,