rs3188996

Orientation

minus

Stabilized

minus

Geno	Mag	Summary
(A;A)	0
(T;T)	0	common in complete genomics

Make rs3188996(C;C)

Make rs3188996(C;T)

Reference

GRCh38 38.1/141

Chromosome

2

Position

113235496

Gene	PAX8, PAX8-AS1

is a	snp
is	mentioned by
dbSNP	rs3188996
dbSNP (classic)	rs3188996
ClinGen	rs3188996
ebi	rs3188996
HLI	rs3188996
Exac	rs3188996
Gnomad	rs3188996
Varsome	rs3188996
LitVar	rs3188996
Map	rs3188996
PheGenI	rs3188996
Biobank	rs3188996
1000 genomes	rs3188996
hgdp	rs3188996
ensembl	rs3188996
geneview	rs3188996
scholar	rs3188996
google	rs3188996
pharmgkb	rs3188996
gwascentral	rs3188996
openSNP	rs3188996
23andMe	rs3188996
SNPshot	rs3188996
SNPdbe	rs3188996
MSV3d	rs3188996
GWAS Ctlg	rs3188996

GMAF

0.006428

Max Magnitude

0

OMIM	167415
Desc	PAX8 POLYMORPHISM
Variant	0001
Related	also

ClinVar
Risk	rs3188996(C;C)
Alt	rs3188996(C;C)
Reference	Rs3188996(T;T)
Significance	Non-pathogenic
Disease	PAX8 POLYMORPHISM
Variation	info
Gene	PAX8 PAX8-AS1
CLNDBN	PAX8 POLYMORPHISM
Reversed	1
HGVS	NC_000002.11:g.113993073A>G
CLNSRC	OMIM Allelic Variant UniProtKB (protein)
CLNACC	RCV000014792.3,