rs397507563

Orientation

minus

Stabilized

minus

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

Make rs397507563(-;-)

Make rs397507563(-;G)

Reference

GRCh38.p7 38.3/150

Chromosome

1

Position

152311184

Gene

FLG

is a	snp
is	mentioned by
dbSNP	rs397507563
dbSNP (classic)	rs397507563
ClinGen	rs397507563
ebi	rs397507563
HLI	rs397507563
Exac	rs397507563
Gnomad	rs397507563
Varsome	rs397507563
LitVar	rs397507563
Map	rs397507563
PheGenI	rs397507563
Biobank	rs397507563
1000 genomes	rs397507563
hgdp	rs397507563
ensembl	rs397507563
geneview	rs397507563
scholar	rs397507563
google	rs397507563
pharmgkb	rs397507563
gwascentral	rs397507563
openSNP	rs397507563
23andMe	rs397507563
SNPshot	rs397507563
SNPdbe	rs397507563
MSV3d	rs397507563
GWAS Ctlg	rs397507563

Max Magnitude

0

ClinVar
Risk	rs397507563(-;-)
Alt	rs397507563(-;-)
Reference	Rs397507563(G;G)
Significance	Pathogenic
Disease	not provided
Variation	info
Gene	FLG
CLNDBN	not provided
Reversed	1
HGVS	NC_000001.10:g.152283660delC
CLNSRC
CLNACC	RCV000479326.1,