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rs2070635

From SNPedia

Orientationplus
Stabilizedplus
Make rs2070635(A;A)
Make rs2070635(A;G)
Make rs2070635(G;G)
ReferenceGRCh38 38.1/141
Chromosome3
Position186618387
GeneAHSG
is asnp
is mentioned by
dbSNPrs2070635
ebirs2070635
HLIrs2070635
Exacrs2070635
Varsomers2070635
Maprs2070635
PheGenIrs2070635
hapmaprs2070635
1000 genomesrs2070635
hgdprs2070635
ensemblrs2070635
gopubmedrs2070635
geneviewrs2070635
scholarrs2070635
googlers2070635
pharmgkbrs2070635
gwascentralrs2070635
openSNPrs2070635
23andMers2070635
23andMe allrs2070635
SNP Nexus

SNPshotrs2070635
SNPdbers2070635
MSV3drs2070635
GWAS Ctlgrs2070635
GMAF0.3903
Max Magnitude
? (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,