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rs4647707

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs4647707(A;A)
Make rs4647707(A;G)
ReferenceGRCh38.p2 38.2/146
Chromosome11
Position47215017
GeneDDB2
is asnp
is mentioned by
dbSNPrs4647707
dbSNP (classic)rs4647707
ClinGenrs4647707
ebirs4647707
HLIrs4647707
Exacrs4647707
Gnomadrs4647707
Varsomers4647707
LitVarrs4647707
Maprs4647707
PheGenIrs4647707
Biobankrs4647707
1000 genomesrs4647707
hgdprs4647707
ensemblrs4647707
geneviewrs4647707
scholarrs4647707
googlers4647707
pharmgkbrs4647707
gwascentralrs4647707
openSNPrs4647707
23andMers4647707
SNPshotrs4647707
SNPdbers4647707
MSV3drs4647707
GWAS Ctlgrs4647707
Max Magnitude0
? (A;A) (A;G) (G;G) 28


[PMID 26650177OA-icon.png] Genetic variations in vitamin D-related pathways and breast cancer risk in African American women in the AMBER Consortium.


ClinVar
Risk rs4647707(A;A)
Alt rs4647707(A;A)
Reference Rs4647707(G;G)
Significance Non-pathogenic
Disease Xeroderma pigmentosum
Variation info
Gene DDB2
CLNDBN Xeroderma pigmentosum
Reversed 0
HGVS NC_000011.9:g.47236568G>A
CLNSRC
CLNACC RCV000402377.1,