rs74129447

Orientation

plus

Stabilized

plus

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

Make rs74129447(C;T)

Make rs74129447(T;T)

Reference

GRCh38.p2 38.2/144

Chromosome

1

Position

152303313

Gene

FLG

is a	snp
is	mentioned by
dbSNP	rs74129447
dbSNP (classic)	rs74129447
ClinGen	rs74129447
ebi	rs74129447
HLI	rs74129447
Exac	rs74129447
Gnomad	rs74129447
Varsome	rs74129447
LitVar	rs74129447
Map	rs74129447
PheGenI	rs74129447
Biobank	rs74129447
1000 genomes	rs74129447
hgdp	rs74129447
ensembl	rs74129447
geneview	rs74129447
scholar	rs74129447
google	rs74129447
pharmgkb	rs74129447
gwascentral	rs74129447
openSNP	rs74129447
23andMe	rs74129447
SNPshot	rs74129447
SNPdbe	rs74129447
MSV3d	rs74129447
GWAS Ctlg	rs74129447

Max Magnitude

0

ClinVar
Risk	rs74129447(A;A) rs74129447(T;T)
Alt	rs74129447(A;A) rs74129447(T;T)
Reference	Rs74129447(C;C)
Significance	Probable-non-pathogenic
Disease	not specified
Variation	info
Gene	FLG
CLNDBN	not specified
Reversed	0
HGVS	NC_000001.10:g.152275789C>T
CLNSRC
CLNACC	RCV000171158.2,