rs782377881

Orientation

plus

Stabilized

plus

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

Make rs782377881(G;T)

Make rs782377881(T;T)

Reference

GRCh38.p7 38.3/150

Chromosome

X

Position

49256801

Gene

FOXP3

is a	snp
is	mentioned by
dbSNP	rs782377881
dbSNP (classic)	rs782377881
ClinGen	rs782377881
ebi	rs782377881
HLI	rs782377881
Exac	rs782377881
Gnomad	rs782377881
Varsome	rs782377881
LitVar	rs782377881
Map	rs782377881
PheGenI	rs782377881
Biobank	rs782377881
1000 genomes	rs782377881
hgdp	rs782377881
ensembl	rs782377881
geneview	rs782377881
scholar	rs782377881
google	rs782377881
pharmgkb	rs782377881
gwascentral	rs782377881
openSNP	rs782377881
23andMe	rs782377881
SNPshot	rs782377881
SNPdbe	rs782377881
MSV3d	rs782377881
GWAS Ctlg	rs782377881

Max Magnitude

0

ClinVar
Risk	rs782377881(A;A) rs782377881(T;T)
Alt	rs782377881(A;A) rs782377881(T;T)
Reference	Rs782377881(G;G)
Significance	Probable-Pathogenic
Disease	not provided
Variation	info
Gene	FOXP3
CLNDBN	not provided
Reversed	0
HGVS	NC_000023.10:g.49113258G>T
CLNSRC
CLNACC	RCV000478450.1,