rs528722713

Orientation

plus

Stabilized

plus

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

Make rs528722713(A;A)

Make rs528722713(A;G)

Reference

GRCh38.p7 38.3/150

Chromosome

1

Position

152307637

Gene

FLG

is a	snp
is	mentioned by
dbSNP	rs528722713
dbSNP (classic)	rs528722713
ClinGen	rs528722713
ebi	rs528722713
HLI	rs528722713
Exac	rs528722713
Gnomad	rs528722713
Varsome	rs528722713
LitVar	rs528722713
Map	rs528722713
PheGenI	rs528722713
Biobank	rs528722713
1000 genomes	rs528722713
hgdp	rs528722713
ensembl	rs528722713
geneview	rs528722713
scholar	rs528722713
google	rs528722713
pharmgkb	rs528722713
gwascentral	rs528722713
openSNP	rs528722713
23andMe	rs528722713
SNPshot	rs528722713
SNPdbe	rs528722713
MSV3d	rs528722713
GWAS Ctlg	rs528722713

Max Magnitude

0

ClinVar
Risk	rs528722713(A;A)
Alt	rs528722713(A;A)
Reference	Rs528722713(G;G)
Significance	Pathogenic
Disease	not provided
Variation	info
Gene	FLG
CLNDBN	not provided
Reversed	0
HGVS	NC_000001.10:g.152280113G>A
CLNSRC
CLNACC	RCV000434890.1,