rs122467171

Orientation

minus

Stabilized

minus

Geno	Mag	Summary
(GAG;GAG)	0	common in clinvar
(GGA;GGA)	0	common/normal

Make rs122467171(-;-)

Make rs122467171(-;GGA)

Reference

GRCh38 38.1/141

Chromosome

X

Position

49255493

Gene

FOXP3

is a	snp
is	mentioned by
dbSNP	rs122467171
dbSNP (classic)	rs122467171
ClinGen	rs122467171
ebi	rs122467171
HLI	rs122467171
Exac	rs122467171
Gnomad	rs122467171
Varsome	rs122467171
LitVar	rs122467171
Map	rs122467171
PheGenI	rs122467171
Biobank	rs122467171
1000 genomes	rs122467171
hgdp	rs122467171
ensembl	rs122467171
geneview	rs122467171
scholar	rs122467171
google	rs122467171
pharmgkb	rs122467171
gwascentral	rs122467171
openSNP	rs122467171
23andMe	rs122467171
SNPshot	rs122467171
SNPdbe	rs122467171
MSV3d	rs122467171
GWAS Ctlg	rs122467171

Max Magnitude

0

OMIM	300292
Desc
Variant	0007
Related	also

ClinVar
Risk	rs122467171(-;-)
Alt	rs122467171(-;-)
Reference	Rs122467171(GAG;GAG)
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.49111954_49111956delTCC
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000012166.11,