rs149484917

Orientation

plus

Stabilized

plus

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

Make rs149484917(C;C)

Make rs149484917(C;G)

Reference

GRCh38.p7 38.3/149

Chromosome

1

Position

152304939

Gene

FLG

is a	snp
is	mentioned by
dbSNP	rs149484917
dbSNP (classic)	rs149484917
ClinGen	rs149484917
ebi	rs149484917
HLI	rs149484917
Exac	rs149484917
Gnomad	rs149484917
Varsome	rs149484917
LitVar	rs149484917
Map	rs149484917
PheGenI	rs149484917
Biobank	rs149484917
1000 genomes	rs149484917
hgdp	rs149484917
ensembl	rs149484917
geneview	rs149484917
scholar	rs149484917
google	rs149484917
pharmgkb	rs149484917
gwascentral	rs149484917
openSNP	rs149484917
23andMe	rs149484917
SNPshot	rs149484917
SNPdbe	rs149484917
MSV3d	rs149484917
GWAS Ctlg	rs149484917

Max Magnitude

0

ClinVar
Risk	rs149484917(C;C)
Alt	rs149484917(C;C)
Reference	Rs149484917(G;G)
Significance	Pathogenic
Disease	not provided
Variation	info
Gene	FLG
CLNDBN	not provided
Reversed	0
HGVS	NC_000001.10:g.152277415G>C
CLNSRC
CLNACC	RCV000293549.2,