rs886037757

Orientation

plus

Stabilized

plus

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

Make rs886037757(-;AC)

Make rs886037757(AC;AC)

Reference

GRCh38.p7 38.3/149

Chromosome

10

Position

100750705

Gene

PAX2

is a	snp
is	mentioned by
dbSNP	rs886037757
dbSNP (classic)	rs886037757
ClinGen	rs886037757
ebi	rs886037757
HLI	rs886037757
Exac	rs886037757
Gnomad	rs886037757
Varsome	rs886037757
LitVar	rs886037757
Map	rs886037757
PheGenI	rs886037757
Biobank	rs886037757
1000 genomes	rs886037757
hgdp	rs886037757
ensembl	rs886037757
geneview	rs886037757
scholar	rs886037757
google	rs886037757
pharmgkb	rs886037757
gwascentral	rs886037757
openSNP	rs886037757
23andMe	rs886037757
SNPshot	rs886037757
SNPdbe	rs886037757
MSV3d	rs886037757
GWAS Ctlg	rs886037757

Max Magnitude

0

ClinVar
Risk	rs886037757(AC;AC)
Alt	rs886037757(AC;AC)
Reference	Rs886037757(-;-)
Significance	Pathogenic
Disease	not provided
Variation	info
Gene	PAX2
CLNDBN	not provided
Reversed	0
HGVS	NC_000010.10:g.102510461_102510462dupAC
CLNSRC
CLNACC	RCV000240626.1,