rs122467173

Orientation

minus

Stabilized

minus

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

Make rs122467173(C;C)

Make rs122467173(C;T)

Reference

GRCh38 38.1/141

Chromosome

X

Position

49253200

Gene

FOXP3

is a	snp
is	mentioned by
dbSNP	rs122467173
dbSNP (classic)	rs122467173
ClinGen	rs122467173
ebi	rs122467173
HLI	rs122467173
Exac	rs122467173
Gnomad	rs122467173
Varsome	rs122467173
LitVar	rs122467173
Map	rs122467173
PheGenI	rs122467173
Biobank	rs122467173
1000 genomes	rs122467173
hgdp	rs122467173
ensembl	rs122467173
geneview	rs122467173
scholar	rs122467173
google	rs122467173
pharmgkb	rs122467173
gwascentral	rs122467173
openSNP	rs122467173
23andMe	rs122467173
SNPshot	rs122467173
SNPdbe	rs122467173
MSV3d	rs122467173
GWAS Ctlg	rs122467173

Max Magnitude

0

OMIM	300292
Desc
Variant	0010
Related	also

ClinVar
Risk	rs122467173(C;C)
Alt	rs122467173(C;C)
Reference	Rs122467173(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.49109661A>G
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000012169.13,