rs122467175

Orientation

minus

Stabilized

minus

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

Make rs122467175(C;C)

Make rs122467175(C;T)

Reference

GRCh38 38.1/141

Chromosome

X

Position

49251711

Gene

FOXP3

is a	snp
is	mentioned by
dbSNP	rs122467175
dbSNP (classic)	rs122467175
ClinGen	rs122467175
ebi	rs122467175
HLI	rs122467175
Exac	rs122467175
Gnomad	rs122467175
Varsome	rs122467175
LitVar	rs122467175
Map	rs122467175
PheGenI	rs122467175
Biobank	rs122467175
1000 genomes	rs122467175
hgdp	rs122467175
ensembl	rs122467175
geneview	rs122467175
scholar	rs122467175
google	rs122467175
pharmgkb	rs122467175
gwascentral	rs122467175
openSNP	rs122467175
23andMe	rs122467175
SNPshot	rs122467175
SNPdbe	rs122467175
MSV3d	rs122467175
GWAS Ctlg	rs122467175

Max Magnitude

0

OMIM	300292
Desc
Variant	0013
Related	also

ClinVar
Risk	rs122467175(C;C)
Alt	rs122467175(C;C)
Reference	Rs122467175(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.49108172A>G
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000012172.11,