rs747453876

Orientation

plus

Stabilized

plus

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

Make rs747453876(C;C)

Make rs747453876(C;T)

Reference

GRCh38.p7 38.3/150

Chromosome

10

Position

100787013

Gene

PAX2

is a	snp
is	mentioned by
dbSNP	rs747453876
dbSNP (classic)	rs747453876
ClinGen	rs747453876
ebi	rs747453876
HLI	rs747453876
Exac	rs747453876
Gnomad	rs747453876
Varsome	rs747453876
LitVar	rs747453876
Map	rs747453876
PheGenI	rs747453876
Biobank	rs747453876
1000 genomes	rs747453876
hgdp	rs747453876
ensembl	rs747453876
geneview	rs747453876
scholar	rs747453876
google	rs747453876
pharmgkb	rs747453876
gwascentral	rs747453876
openSNP	rs747453876
23andMe	rs747453876
SNPshot	rs747453876
SNPdbe	rs747453876
MSV3d	rs747453876
GWAS Ctlg	rs747453876

Max Magnitude

0

ClinVar
Risk	rs747453876(C;C)
Alt	rs747453876(C;C)
Reference	Rs747453876(T;T)
Significance	Pathogenic
Disease	not provided
Variation	info
Gene	PAX2
CLNDBN	not provided
Reversed	0
HGVS	NC_000010.10:g.102546770T>C
CLNSRC
CLNACC	RCV000483686.1,