rs764094665

Orientation

plus

Stabilized

plus

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

Make rs764094665(A;A)

Make rs764094665(A;T)

Reference

GRCh38.p7 38.3/149

Chromosome

1

Position

152304562

Gene

FLG

is a	snp
is	mentioned by
dbSNP	rs764094665
dbSNP (classic)	rs764094665
ClinGen	rs764094665
ebi	rs764094665
HLI	rs764094665
Exac	rs764094665
Gnomad	rs764094665
Varsome	rs764094665
LitVar	rs764094665
Map	rs764094665
PheGenI	rs764094665
Biobank	rs764094665
1000 genomes	rs764094665
hgdp	rs764094665
ensembl	rs764094665
geneview	rs764094665
scholar	rs764094665
google	rs764094665
pharmgkb	rs764094665
gwascentral	rs764094665
openSNP	rs764094665
23andMe	rs764094665
SNPshot	rs764094665
SNPdbe	rs764094665
MSV3d	rs764094665
GWAS Ctlg	rs764094665

Max Magnitude

0

ClinVar
Risk	rs764094665(A;A)
Alt	rs764094665(A;A)
Reference	Rs764094665(T;T)
Significance	Pathogenic
Disease	not provided
Variation	info
Gene	FLG
CLNDBN	not provided
Reversed	0
HGVS	NC_000001.10:g.152277038T>A
CLNSRC
CLNACC	RCV000254718.1,