rs763369315

Orientation

plus

Stabilized

plus

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

Make rs763369315(C;T)

Make rs763369315(T;T)

Reference

GRCh38.p2 38.2/144

Chromosome

19

Position

35285003

Gene

HAMP

is a	snp
is	mentioned by
dbSNP	rs763369315
dbSNP (classic)	rs763369315
ClinGen	rs763369315
ebi	rs763369315
HLI	rs763369315
Exac	rs763369315
Gnomad	rs763369315
Varsome	rs763369315
LitVar	rs763369315
Map	rs763369315
PheGenI	rs763369315
Biobank	rs763369315
1000 genomes	rs763369315
hgdp	rs763369315
ensembl	rs763369315
geneview	rs763369315
scholar	rs763369315
google	rs763369315
pharmgkb	rs763369315
gwascentral	rs763369315
openSNP	rs763369315
23andMe	rs763369315
SNPshot	rs763369315
SNPdbe	rs763369315
MSV3d	rs763369315
GWAS Ctlg	rs763369315

Max Magnitude

0

ClinVar
Risk	rs763369315(A;A) rs763369315(T;T)
Alt	rs763369315(A;A) rs763369315(T;T)
Reference	Rs763369315(C;C)
Significance	Pathogenic
Disease	Hemochromatosis type 1
Variation	info
Gene	HAMP
CLNDBN	Hemochromatosis type 1
Reversed	0
HGVS	NC_000019.9:g.35775906C>A
CLNSRC
CLNACC	RCV000167903.1,