rs886037754

Orientation

plus

Stabilized

plus

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

Make rs886037754(-;-)

Make rs886037754(-;GC)

Reference

GRCh38.p7 38.3/149

Chromosome

10

Position

100749821

Gene

PAX2

is a	snp
is	mentioned by
dbSNP	rs886037754
dbSNP (classic)	rs886037754
ClinGen	rs886037754
ebi	rs886037754
HLI	rs886037754
Exac	rs886037754
Gnomad	rs886037754
Varsome	rs886037754
LitVar	rs886037754
Map	rs886037754
PheGenI	rs886037754
Biobank	rs886037754
1000 genomes	rs886037754
hgdp	rs886037754
ensembl	rs886037754
geneview	rs886037754
scholar	rs886037754
google	rs886037754
pharmgkb	rs886037754
gwascentral	rs886037754
openSNP	rs886037754
23andMe	rs886037754
SNPshot	rs886037754
SNPdbe	rs886037754
MSV3d	rs886037754
GWAS Ctlg	rs886037754

Max Magnitude

0

ClinVar
Risk	rs886037754(-;-)
Alt	rs886037754(-;-)
Reference	Rs886037754(GC;GC)
Significance	Pathogenic
Disease	not provided
Variation	info
Gene	PAX2
CLNDBN	not provided
Reversed	0
HGVS	NC_000010.10:g.102509578_102509579delGC
CLNSRC
CLNACC	RCV000240627.1,