rs121917718

Orientation

minus

Stabilized

minus

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

Make rs121917718(C;T)

Make rs121917718(T;T)

Reference

GRCh38 38.1/141

Chromosome

7

Position

127613804

Gene

PAX4

is a	snp
is	mentioned by
dbSNP	rs121917718
dbSNP (classic)	rs121917718
ClinGen	rs121917718
ebi	rs121917718
HLI	rs121917718
Exac	rs121917718
Gnomad	rs121917718
Varsome	rs121917718
LitVar	rs121917718
Map	rs121917718
PheGenI	rs121917718
Biobank	rs121917718
1000 genomes	rs121917718
hgdp	rs121917718
ensembl	rs121917718
geneview	rs121917718
scholar	rs121917718
google	rs121917718
pharmgkb	rs121917718
gwascentral	rs121917718
openSNP	rs121917718
23andMe	rs121917718
SNPshot	rs121917718
SNPdbe	rs121917718
MSV3d	rs121917718
GWAS Ctlg	rs121917718

Max Magnitude

0

OMIM	167413
Desc
Variant	0004
Related	also

ClinVar
Risk	rs121917718(T;T)
Alt	rs121917718(T;T)
Reference	Rs121917718(C;C)
Significance	Pathogenic
Disease	Maturity-onset diabetes of the young
Variation	info
Gene	PAX4
CLNDBN	Maturity-onset diabetes of the young, type 9
Reversed	1
HGVS	NC_000007.13:g.127253858G>A
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000014803.25,