rs374588791

Orientation

plus

Stabilized

plus

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

Make rs374588791(C;T)

Make rs374588791(T;T)

Reference

GRCh38.p7 38.3/149

Chromosome

1

Position

152307622

Gene

FLG

is a	snp
is	mentioned by
dbSNP	rs374588791
dbSNP (classic)	rs374588791
ClinGen	rs374588791
ebi	rs374588791
HLI	rs374588791
Exac	rs374588791
Gnomad	rs374588791
Varsome	rs374588791
LitVar	rs374588791
Map	rs374588791
PheGenI	rs374588791
Biobank	rs374588791
1000 genomes	rs374588791
hgdp	rs374588791
ensembl	rs374588791
geneview	rs374588791
scholar	rs374588791
google	rs374588791
pharmgkb	rs374588791
gwascentral	rs374588791
openSNP	rs374588791
23andMe	rs374588791
SNPshot	rs374588791
SNPdbe	rs374588791
MSV3d	rs374588791
GWAS Ctlg	rs374588791

Max Magnitude

0

ClinVar
Risk	rs374588791(A;A) rs374588791(T;T)
Alt	rs374588791(A;A) rs374588791(T;T)
Reference	Rs374588791(C;C)
Significance	Pathogenic
Disease	not provided
Variation	info
Gene	FLG
CLNDBN	not provided
Reversed	0
HGVS	NC_000001.10:g.152280098C>A
CLNSRC
CLNACC	RCV000255031.1,