rs546871592

Orientation

plus

Stabilized

plus

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

Make rs546871592(A;A)

Make rs546871592(A;G)

Reference

GRCh38.p7 38.3/150

Chromosome

1

Position

152303251

Gene

FLG

is a	snp
is	mentioned by
dbSNP	rs546871592
dbSNP (classic)	rs546871592
ClinGen	rs546871592
ebi	rs546871592
HLI	rs546871592
Exac	rs546871592
Gnomad	rs546871592
Varsome	rs546871592
LitVar	rs546871592
Map	rs546871592
PheGenI	rs546871592
Biobank	rs546871592
1000 genomes	rs546871592
hgdp	rs546871592
ensembl	rs546871592
geneview	rs546871592
scholar	rs546871592
google	rs546871592
pharmgkb	rs546871592
gwascentral	rs546871592
openSNP	rs546871592
23andMe	rs546871592
SNPshot	rs546871592
SNPdbe	rs546871592
MSV3d	rs546871592
GWAS Ctlg	rs546871592

Max Magnitude

0

ClinVar
Risk	rs546871592(A;A)
Alt	rs546871592(A;A)
Reference	Rs546871592(G;G)
Significance	Probable-Pathogenic
Disease	not provided
Variation	info
Gene	FLG
CLNDBN	not provided
Reversed	0
HGVS	NC_000001.10:g.152275727G>A
CLNSRC
CLNACC	RCV000493665.1,