rs756998312

Orientation

plus

Stabilized

plus

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

Make rs756998312(A;A)

Make rs756998312(A;G)

Reference

GRCh38.p7 38.3/149

Chromosome

1

Position

152310100

Gene

FLG

is a	snp
is	mentioned by
dbSNP	rs756998312
dbSNP (classic)	rs756998312
ClinGen	rs756998312
ebi	rs756998312
HLI	rs756998312
Exac	rs756998312
Gnomad	rs756998312
Varsome	rs756998312
LitVar	rs756998312
Map	rs756998312
PheGenI	rs756998312
Biobank	rs756998312
1000 genomes	rs756998312
hgdp	rs756998312
ensembl	rs756998312
geneview	rs756998312
scholar	rs756998312
google	rs756998312
pharmgkb	rs756998312
gwascentral	rs756998312
openSNP	rs756998312
23andMe	rs756998312
SNPshot	rs756998312
SNPdbe	rs756998312
MSV3d	rs756998312
GWAS Ctlg	rs756998312

Max Magnitude

0

ClinVar
Risk	rs756998312(A;A) rs756998312(T;T)
Alt	rs756998312(A;A) rs756998312(T;T)
Reference	Rs756998312(G;G)
Significance	Pathogenic
Disease	not provided
Variation	info
Gene	FLG
CLNDBN	not provided
Reversed	0
HGVS	NC_000001.10:g.152282576G>A
CLNSRC
CLNACC	RCV000323173.1,