rs886037756

Orientation

plus

Stabilized

plus

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

Make rs886037756(-;GTGAACC)

Make rs886037756(GTGAACC;GTGAACC)

Reference

GRCh38.p7 38.3/149

Chromosome

10

Position

100749759

Gene

PAX2

is a	snp
is	mentioned by
dbSNP	rs886037756
dbSNP (classic)	rs886037756
ClinGen	rs886037756
ebi	rs886037756
HLI	rs886037756
Exac	rs886037756
Gnomad	rs886037756
Varsome	rs886037756
LitVar	rs886037756
Map	rs886037756
PheGenI	rs886037756
Biobank	rs886037756
1000 genomes	rs886037756
hgdp	rs886037756
ensembl	rs886037756
geneview	rs886037756
scholar	rs886037756
google	rs886037756
pharmgkb	rs886037756
gwascentral	rs886037756
openSNP	rs886037756
23andMe	rs886037756
SNPshot	rs886037756
SNPdbe	rs886037756
MSV3d	rs886037756
GWAS Ctlg	rs886037756

Max Magnitude

0

ClinVar
Risk	rs886037756(GTGAACC;GTGAACC)
Alt	rs886037756(GTGAACC;GTGAACC)
Reference	Rs886037756(-;-)
Significance	Pathogenic
Disease	not provided
Variation	info
Gene	PAX2
CLNDBN	not provided
Reversed	0
HGVS	NC_000010.10:g.102509516_102509517insGTGAACC
CLNSRC
CLNACC	RCV000240647.1,