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rs112832879

From SNPedia
Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs112832879(A;A)
Make rs112832879(A;G)
ReferenceGRCh38.p7 38.3/150
Chromosome3
Position10043483
GeneFANCD2
is asnp
is mentioned by
dbSNPrs112832879
dbSNP (old)rs112832879
ClinGenrs112832879
ebirs112832879
HLIrs112832879
Exacrs112832879
Gnomadrs112832879
Varsomers112832879
Maprs112832879
PheGenIrs112832879
Biobankrs112832879
1000 genomesrs112832879
hgdprs112832879
ensemblrs112832879
gopubmedrs112832879
geneviewrs112832879
scholarrs112832879
googlers112832879
pharmgkbrs112832879
gwascentralrs112832879
openSNPrs112832879
23andMers112832879
23andMe allrs112832879
SNPshotrs112832879
SNPdbers112832879
MSV3drs112832879
GWAS Ctlgrs112832879
Max Magnitude0
ClinVar
Risk rs112832879(A;A)
Alt rs112832879(A;A)
Reference Rs112832879(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene FANCD2
CLNDBN not provided
Reversed 0
HGVS NC_000003.11:g.10085167G>A
CLNSRC
CLNACC RCV000421802.1,