rs122467174

Orientation

minus

Stabilized

minus

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

Make rs122467174(A;A)

Make rs122467174(A;G)

Reference

GRCh38 38.1/141

Chromosome

X

Position

49258503

Gene

FOXP3

is a	snp
is	mentioned by
dbSNP	rs122467174
dbSNP (classic)	rs122467174
ClinGen	rs122467174
ebi	rs122467174
HLI	rs122467174
Exac	rs122467174
Gnomad	rs122467174
Varsome	rs122467174
LitVar	rs122467174
Map	rs122467174
PheGenI	rs122467174
Biobank	rs122467174
1000 genomes	rs122467174
hgdp	rs122467174
ensembl	rs122467174
geneview	rs122467174
scholar	rs122467174
google	rs122467174
pharmgkb	rs122467174
gwascentral	rs122467174
openSNP	rs122467174
23andMe	rs122467174
SNPshot	rs122467174
SNPdbe	rs122467174
MSV3d	rs122467174
GWAS Ctlg	rs122467174

Max Magnitude

0

OMIM	300292
Desc
Variant	0012
Related	also

ClinVar
Risk	rs122467174(A;A)
Alt	rs122467174(A;A)
Reference	Rs122467174(G;G)
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.49114960C>T
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000012171.11,