Have questions? Visit https://www.reddit.com/r/SNPedia

rs104893751

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in complete genomics
Make rs104893751(A;A)
Make rs104893751(A;G)
ReferenceGRCh38 38.1/141
Chromosome3
Position9750423
GeneOGG1
is asnp
is mentioned by
dbSNPrs104893751
ebirs104893751
HLIrs104893751
Exacrs104893751
Varsomers104893751
Maprs104893751
PheGenIrs104893751
hapmaprs104893751
1000 genomesrs104893751
hgdprs104893751
ensemblrs104893751
gopubmedrs104893751
geneviewrs104893751
scholarrs104893751
googlers104893751
pharmgkbrs104893751
gwascentralrs104893751
openSNPrs104893751
23andMers104893751
23andMe allrs104893751
SNP Nexus

SNPshotrs104893751
SNPdbers104893751
MSV3drs104893751
GWAS Ctlgrs104893751
GMAF0.0004591
Max Magnitude0
OMIM601982
Desc
Variant0001
Relatedalso
ClinVar
Risk rs104893751(A;A)
Alt rs104893751(A;A)
Reference rs104893751(G;G)
Significance Pathogenic
Disease Clear cell carcinoma of kidney
Variation info
Gene OGG1
CLNDBN Clear cell carcinoma of kidney
Reversed 0
HGVS NC_000003.11:g.9792107G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000008040.4,