rs869312928

Orientation

plus

Stabilized

plus

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

Make rs869312928(A;G)

Make rs869312928(G;G)

Reference

GRCh38.p2 38.2/147

Chromosome

1

Position

109627893

Gene

AMPD2

is a	snp
is	mentioned by
dbSNP	rs869312928
dbSNP (classic)	rs869312928
ClinGen	rs869312928
ebi	rs869312928
HLI	rs869312928
Exac	rs869312928
Gnomad	rs869312928
Varsome	rs869312928
LitVar	rs869312928
Map	rs869312928
PheGenI	rs869312928
Biobank	rs869312928
1000 genomes	rs869312928
hgdp	rs869312928
ensembl	rs869312928
geneview	rs869312928
scholar	rs869312928
google	rs869312928
pharmgkb	rs869312928
gwascentral	rs869312928
openSNP	rs869312928
23andMe	rs869312928
SNPshot	rs869312928
SNPdbe	rs869312928
MSV3d	rs869312928
GWAS Ctlg	rs869312928

Max Magnitude

0

ClinVar
Risk	rs869312928(G;G)
Alt	rs869312928(G;G)
Reference	Rs869312928(A;A)
Significance	Probable-Pathogenic
Disease	Inborn genetic diseases
Variation	info
Gene	AMPD2
CLNDBN	Inborn genetic diseases
Reversed	0
HGVS	NC_000001.10:g.110170515A>G
CLNSRC
CLNACC	RCV000210639.1,