rs148606936

Orientation

plus

Stabilized

plus

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

Make rs148606936(A;A)

Make rs148606936(A;G)

Reference

GRCh38.p7 38.3/149

Chromosome

1

Position

152303434

Gene

FLG

is a	snp
is	mentioned by
dbSNP	rs148606936
dbSNP (classic)	rs148606936
ClinGen	rs148606936
ebi	rs148606936
HLI	rs148606936
Exac	rs148606936
Gnomad	rs148606936
Varsome	rs148606936
LitVar	rs148606936
Map	rs148606936
PheGenI	rs148606936
Biobank	rs148606936
1000 genomes	rs148606936
hgdp	rs148606936
ensembl	rs148606936
geneview	rs148606936
scholar	rs148606936
google	rs148606936
pharmgkb	rs148606936
gwascentral	rs148606936
openSNP	rs148606936
23andMe	rs148606936
SNPshot	rs148606936
SNPdbe	rs148606936
MSV3d	rs148606936
GWAS Ctlg	rs148606936

Max Magnitude

0

ClinVar
Risk	rs148606936(A;A) rs148606936(T;T)
Alt	rs148606936(A;A) rs148606936(T;T)
Reference	Rs148606936(G;G)
Significance	Pathogenic
Disease	not provided
Variation	info
Gene	FLG
CLNDBN	not provided
Reversed	0
HGVS	NC_000001.10:g.152275910G>A
CLNSRC
CLNACC	RCV000365311.1,