rs797044859

Orientation

plus

Stabilized

plus

Geno	Mag	Summary
(AT;AT)	0	common in clinvar
(I;I)	0	common genotype

Make rs797044859(-;-)

Make rs797044859(-;AT)

Reference

GRCh38.p2 38.2/146

Chromosome

6

Position

157200765

Gene

ARID1B

is a	snp
is	mentioned by
dbSNP	rs797044859
dbSNP (classic)	rs797044859
ClinGen	rs797044859
ebi	rs797044859
HLI	rs797044859
Exac	rs797044859
Gnomad	rs797044859
Varsome	rs797044859
LitVar	rs797044859
Map	rs797044859
PheGenI	rs797044859
Biobank	rs797044859
1000 genomes	rs797044859
hgdp	rs797044859
ensembl	rs797044859
geneview	rs797044859
scholar	rs797044859
google	rs797044859
pharmgkb	rs797044859
gwascentral	rs797044859
openSNP	rs797044859
23andMe	rs797044859
SNPshot	rs797044859
SNPdbe	rs797044859
MSV3d	rs797044859
GWAS Ctlg	rs797044859

Max Magnitude

0

ClinVar
Risk	rs797044859(-;-)
Alt	rs797044859(-;-)
Reference	Rs797044859(AT;AT)
Significance	Pathogenic
Disease	Inborn genetic diseases
Variation	info
Gene	ARID1B
CLNDBN	Inborn genetic diseases
Reversed	0
HGVS	NC_000006.11:g.157521899_157521900delAT
CLNSRC
CLNACC	RCV000190662.1,