rs2070635

Orientation

plus

Stabilized

plus

Make rs2070635(A;A)

Make rs2070635(A;G)

Make rs2070635(G;G)

Reference

GRCh38 38.1/141

Chromosome

3

Position

186618387

Gene

AHSG

is a	snp
is	mentioned by
dbSNP	rs2070635
dbSNP (classic)	rs2070635
ClinGen	rs2070635
ebi	rs2070635
HLI	rs2070635
Exac	rs2070635
Gnomad	rs2070635
Varsome	rs2070635
LitVar	rs2070635
Map	rs2070635
PheGenI	rs2070635
Biobank	rs2070635
1000 genomes	rs2070635
hgdp	rs2070635
ensembl	rs2070635
geneview	rs2070635
scholar	rs2070635
google	rs2070635
pharmgkb	rs2070635
gwascentral	rs2070635
openSNP	rs2070635
23andMe	rs2070635
SNPshot	rs2070635
SNPdbe	rs2070635
MSV3d	rs2070635
GWAS Ctlg	rs2070635

GMAF

0.3903

Max Magnitude

0

?	(A;A) (A;G) (G;G)	28

[PMID 19358088] AHSG Gene Variation is not Associated with Regional Body Fat Distribution - A Magnetic Resonance Study.

[PMID 20031641] Association of AHSG Gene Polymorphisms With Fetuin-A Plasma Levels and Cardiovascular Diseases in the EPIC-Potsdam Study

ClinVar
Risk	rs2070635(G;G)
Alt	rs2070635(G;G)
Reference	rs2070635(A;A)
Significance	Other
Disease	Calcium oxalate urolithiasis
Variation	info
Gene	AHSG
CLNDBN	Calcium oxalate urolithiasis
Reversed	0
HGVS	NC_000003.11:g.186336176A>G
CLNSRC	ClinVar
CLNACC	RCV000128584.1,