rs1057518212

Orientation

minus

Stabilized

minus

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

Make rs1057518212(C;G)

Make rs1057518212(G;G)

Reference

GRCh38.p7 38.3/150

Chromosome

1

Position

152303358

Gene

FLG

is a	snp
is	mentioned by
dbSNP	rs1057518212
dbSNP (classic)	rs1057518212
ClinGen	rs1057518212
ebi	rs1057518212
HLI	rs1057518212
Exac	rs1057518212
Gnomad	rs1057518212
Varsome	rs1057518212
LitVar	rs1057518212
Map	rs1057518212
PheGenI	rs1057518212
Biobank	rs1057518212
1000 genomes	rs1057518212
hgdp	rs1057518212
ensembl	rs1057518212
geneview	rs1057518212
scholar	rs1057518212
google	rs1057518212
pharmgkb	rs1057518212
gwascentral	rs1057518212
openSNP	rs1057518212
23andMe	rs1057518212
SNPshot	rs1057518212
SNPdbe	rs1057518212
MSV3d	rs1057518212
GWAS Ctlg	rs1057518212

Max Magnitude

0

ClinVar
Risk	rs1057518212(G;G)
Alt	rs1057518212(G;G)
Reference	Rs1057518212(C;C)
Significance	Pathogenic
Disease	not provided
Variation	info
Gene	FLG
CLNDBN	not provided
Reversed	1
HGVS	NC_000001.10:g.152275834G>C
CLNSRC
CLNACC	RCV000412869.1,