rs147145234

Orientation

plus

Stabilized

plus

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

Make rs147145234(G;T)

Make rs147145234(T;T)

Reference

GRCh38.p2 38.2/147

Chromosome

1

Position

152308647

Gene

FLG

is a	snp
is	mentioned by
dbSNP	rs147145234
dbSNP (classic)	rs147145234
ClinGen	rs147145234
ebi	rs147145234
HLI	rs147145234
Exac	rs147145234
Gnomad	rs147145234
Varsome	rs147145234
LitVar	rs147145234
Map	rs147145234
PheGenI	rs147145234
Biobank	rs147145234
1000 genomes	rs147145234
hgdp	rs147145234
ensembl	rs147145234
geneview	rs147145234
scholar	rs147145234
google	rs147145234
pharmgkb	rs147145234
gwascentral	rs147145234
openSNP	rs147145234
23andMe	rs147145234
SNPshot	rs147145234
SNPdbe	rs147145234
MSV3d	rs147145234
GWAS Ctlg	rs147145234

Max Magnitude

0

ClinVar
Risk	rs147145234(T;T)
Alt	rs147145234(T;T)
Reference	Rs147145234(G;G)
Significance	Pathogenic
Disease	Inborn genetic diseases
Variation	info
Gene	FLG
CLNDBN	Inborn genetic diseases
Reversed	0
HGVS	NC_000001.10:g.152281123G>T
CLNSRC
CLNACC	RCV000210631.1,