rs104894696

Orientation

plus

Stabilized

plus

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

Make rs104894696(A;A)

Make rs104894696(A;G)

Reference

GRCh38 38.1/141

Chromosome

19

Position

35284999

Gene

HAMP

is a	snp
is	mentioned by
dbSNP	rs104894696
dbSNP (classic)	rs104894696
ClinGen	rs104894696
ebi	rs104894696
HLI	rs104894696
Exac	rs104894696
Gnomad	rs104894696
Varsome	rs104894696
LitVar	rs104894696
Map	rs104894696
PheGenI	rs104894696
Biobank	rs104894696
1000 genomes	rs104894696
hgdp	rs104894696
ensembl	rs104894696
geneview	rs104894696
scholar	rs104894696
google	rs104894696
pharmgkb	rs104894696
gwascentral	rs104894696
openSNP	rs104894696
23andMe	rs104894696
SNPshot	rs104894696
SNPdbe	rs104894696
MSV3d	rs104894696
GWAS Ctlg	rs104894696

GMAF

0.0004591

Max Magnitude

0

OMIM	606464
Desc
Variant	0004
Related	also

ClinVar
Risk	rs104894696(A;A)
Alt	rs104894696(A;A)
Reference	Rs104894696(G;G)
Significance	Other
Disease	Hemochromatosis Hemochromatosis type 1
Variation	info
Gene	HAMP
CLNDBN	Hemochromatosis, type 2a, modifier of Hemochromatosis type 1
Reversed	0
HGVS	NC_000019.9:g.35775902G>A
CLNSRC	OMIM Allelic Variant UniProtKB (protein)
CLNACC	RCV000004507.4, RCV000205666.2,