rs749083759

Orientation

plus

Stabilized

plus

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

Make rs749083759(A;A)

Make rs749083759(A;G)

Reference

GRCh38.p7 38.3/150

Chromosome

1

Position

152303917

Gene

FLG

is a	snp
is	mentioned by
dbSNP	rs749083759
dbSNP (classic)	rs749083759
ClinGen	rs749083759
ebi	rs749083759
HLI	rs749083759
Exac	rs749083759
Gnomad	rs749083759
Varsome	rs749083759
LitVar	rs749083759
Map	rs749083759
PheGenI	rs749083759
Biobank	rs749083759
1000 genomes	rs749083759
hgdp	rs749083759
ensembl	rs749083759
geneview	rs749083759
scholar	rs749083759
google	rs749083759
pharmgkb	rs749083759
gwascentral	rs749083759
openSNP	rs749083759
23andMe	rs749083759
SNPshot	rs749083759
SNPdbe	rs749083759
MSV3d	rs749083759
GWAS Ctlg	rs749083759

Max Magnitude

0

ClinVar
Risk	rs749083759(A;A) rs749083759(C;C)
Alt	rs749083759(A;A) rs749083759(C;C)
Reference	Rs749083759(G;G)
Significance	Pathogenic
Disease	not provided
Variation	info
Gene	FLG
CLNDBN	not provided
Reversed	0
HGVS	NC_000001.10:g.152276393G>A
CLNSRC
CLNACC	RCV000493067.1,