rs122467169

Orientation

minus

Stabilized

minus

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

Make rs122467169(G;G)

Make rs122467169(G;T)

Reference

GRCh38 38.1/141

Chromosome

X

Position

49251698

Gene

FOXP3

is a	snp
is	mentioned by
dbSNP	rs122467169
dbSNP (classic)	rs122467169
ClinGen	rs122467169
ebi	rs122467169
HLI	rs122467169
Exac	rs122467169
Gnomad	rs122467169
Varsome	rs122467169
LitVar	rs122467169
Map	rs122467169
PheGenI	rs122467169
Biobank	rs122467169
1000 genomes	rs122467169
hgdp	rs122467169
ensembl	rs122467169
geneview	rs122467169
scholar	rs122467169
google	rs122467169
pharmgkb	rs122467169
gwascentral	rs122467169
openSNP	rs122467169
23andMe	rs122467169
SNPshot	rs122467169
SNPdbe	rs122467169
MSV3d	rs122467169
GWAS Ctlg	rs122467169

Max Magnitude

0

OMIM	300292
Desc
Variant	0003
Related	also

ClinVar
Risk	rs122467169(G;G)
Alt	rs122467169(G;G)
Reference	Rs122467169(T;T)
Significance	Pathogenic
Disease	Insulin-dependent diabetes mellitus secretory diarrhea syndrome
Variation	info
Gene	FOXP3
CLNDBN	Insulin-dependent diabetes mellitus secretory diarrhea syndrome
Reversed	1
HGVS	NC_000023.10:g.49108159A>C
CLNSRC	OMIM Allelic Variant UniProtKB (protein)
CLNACC	RCV000012162.13,