rs199895224

Orientation

plus

Stabilized

plus

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

Make rs199895224(A;A)

Make rs199895224(A;C)

Reference

GRCh38.p7 38.3/150

Chromosome

1

Position

152311129

Gene

FLG

is a	snp
is	mentioned by
dbSNP	rs199895224
dbSNP (classic)	rs199895224
ClinGen	rs199895224
ebi	rs199895224
HLI	rs199895224
Exac	rs199895224
Gnomad	rs199895224
Varsome	rs199895224
LitVar	rs199895224
Map	rs199895224
PheGenI	rs199895224
Biobank	rs199895224
1000 genomes	rs199895224
hgdp	rs199895224
ensembl	rs199895224
geneview	rs199895224
scholar	rs199895224
google	rs199895224
pharmgkb	rs199895224
gwascentral	rs199895224
openSNP	rs199895224
23andMe	rs199895224
SNPshot	rs199895224
SNPdbe	rs199895224
MSV3d	rs199895224
GWAS Ctlg	rs199895224

Max Magnitude

0

ClinVar
Risk	rs199895224(A;A)
Alt	rs199895224(A;A)
Reference	Rs199895224(C;C)
Significance	Pathogenic
Disease	not provided
Variation	info
Gene	FLG
CLNDBN	not provided
Reversed	0
HGVS	NC_000001.10:g.152283605C>A
CLNSRC
CLNACC	RCV000414116.1,