rs886037755

Orientation

plus

Stabilized

plus

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

Make rs886037755(A;A)

Make rs886037755(A;G)

Reference

GRCh38.p7 38.3/149

Chromosome

10

Position

100749889

Gene

PAX2

is a	snp
is	mentioned by
dbSNP	rs886037755
dbSNP (classic)	rs886037755
ClinGen	rs886037755
ebi	rs886037755
HLI	rs886037755
Exac	rs886037755
Gnomad	rs886037755
Varsome	rs886037755
LitVar	rs886037755
Map	rs886037755
PheGenI	rs886037755
Biobank	rs886037755
1000 genomes	rs886037755
hgdp	rs886037755
ensembl	rs886037755
geneview	rs886037755
scholar	rs886037755
google	rs886037755
pharmgkb	rs886037755
gwascentral	rs886037755
openSNP	rs886037755
23andMe	rs886037755
SNPshot	rs886037755
SNPdbe	rs886037755
MSV3d	rs886037755
GWAS Ctlg	rs886037755

Max Magnitude

0

ClinVar
Risk	rs886037755(A;A)
Alt	rs886037755(A;A)
Reference	Rs886037755(G;G)
Significance	Pathogenic
Disease	not provided
Variation	info
Gene	PAX2
CLNDBN	not provided
Reversed	0
HGVS	NC_000010.10:g.102509646G>A
CLNSRC
CLNACC	RCV000240634.1,