rs1057516168

Orientation

minus

Stabilized

minus

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

Make rs1057516168(A;G)

Make rs1057516168(G;G)

Reference

GRCh38.p7 38.3/150

Chromosome

3

Position

138946079

Gene	FOXL2, FOXL2NB

is a	snp
is	mentioned by
dbSNP	rs1057516168
dbSNP (classic)	rs1057516168
ClinGen	rs1057516168
ebi	rs1057516168
HLI	rs1057516168
Exac	rs1057516168
Gnomad	rs1057516168
Varsome	rs1057516168
LitVar	rs1057516168
Map	rs1057516168
PheGenI	rs1057516168
Biobank	rs1057516168
1000 genomes	rs1057516168
hgdp	rs1057516168
ensembl	rs1057516168
geneview	rs1057516168
scholar	rs1057516168
google	rs1057516168
pharmgkb	rs1057516168
gwascentral	rs1057516168
openSNP	rs1057516168
23andMe	rs1057516168
SNPshot	rs1057516168
SNPdbe	rs1057516168
MSV3d	rs1057516168
GWAS Ctlg	rs1057516168

Max Magnitude

0

ClinVar
Risk	rs1057516168(G;G)
Alt	rs1057516168(G;G)
Reference	Rs1057516168(A;A)
Significance	Pathogenic
Disease	Blepharophimosis
Variation	info
Gene	FOXL2 FOXL2NB C3orf72
CLNDBN	Blepharophimosis, ptosis, and epicanthus inversus
Reversed	1
HGVS	NC_000003.11:g.138664921T>C
CLNSRC
CLNACC	RCV000408786.1,