rs201356558

Orientation

plus

Stabilized

plus

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

Make rs201356558(A;A)

Make rs201356558(A;G)

Reference

GRCh38.p7 38.3/149

Chromosome

1

Position

152304661

Gene

FLG

is a	snp
is	mentioned by
dbSNP	rs201356558
dbSNP (classic)	rs201356558
ClinGen	rs201356558
ebi	rs201356558
HLI	rs201356558
Exac	rs201356558
Gnomad	rs201356558
Varsome	rs201356558
LitVar	rs201356558
Map	rs201356558
PheGenI	rs201356558
Biobank	rs201356558
1000 genomes	rs201356558
hgdp	rs201356558
ensembl	rs201356558
geneview	rs201356558
scholar	rs201356558
google	rs201356558
pharmgkb	rs201356558
gwascentral	rs201356558
openSNP	rs201356558
23andMe	rs201356558
SNPshot	rs201356558
SNPdbe	rs201356558
MSV3d	rs201356558
GWAS Ctlg	rs201356558

Max Magnitude

0

ClinVar
Risk	rs201356558(A;A) rs201356558(C;C)
Alt	rs201356558(A;A) rs201356558(C;C)
Reference	Rs201356558(G;G)
Significance	Pathogenic
Disease	not provided
Variation	info
Gene	FLG
CLNDBN	not provided
Reversed	0
HGVS	NC_000001.10:g.152277137G>A
CLNSRC
CLNACC	RCV000255606.1,