rs1057518148

Orientation

minus

Stabilized

minus

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

Make rs1057518148(C;T)

Make rs1057518148(T;T)

Reference

GRCh38.p7 38.3/150

Chromosome

1

Position

152309656

Gene

FLG

is a	snp
is	mentioned by
dbSNP	rs1057518148
dbSNP (classic)	rs1057518148
ClinGen	rs1057518148
ebi	rs1057518148
HLI	rs1057518148
Exac	rs1057518148
Gnomad	rs1057518148
Varsome	rs1057518148
LitVar	rs1057518148
Map	rs1057518148
PheGenI	rs1057518148
Biobank	rs1057518148
1000 genomes	rs1057518148
hgdp	rs1057518148
ensembl	rs1057518148
geneview	rs1057518148
scholar	rs1057518148
google	rs1057518148
pharmgkb	rs1057518148
gwascentral	rs1057518148
openSNP	rs1057518148
23andMe	rs1057518148
SNPshot	rs1057518148
SNPdbe	rs1057518148
MSV3d	rs1057518148
GWAS Ctlg	rs1057518148

Max Magnitude

0

ClinVar
Risk	rs1057518148(T;T)
Alt	rs1057518148(T;T)
Reference	Rs1057518148(C;C)
Significance	Pathogenic
Disease	not provided
Variation	info
Gene	FLG
CLNDBN	not provided
Reversed	1
HGVS	NC_000001.10:g.152282132G>A
CLNSRC
CLNACC	RCV000414080.1,