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rs869312805

From SNPedia

Orientationplus
Geno Mag Summary
(CCT;CCT) 0 common in clinvar
Make rs869312805(-;-)
Make rs869312805(-;CCT)
ReferenceGRCh38.p2 38.2/147
Chromosome3
Position10064804
GeneFANCD2
is asnp
is mentioned by
dbSNPrs869312805
ebirs869312805
HLIrs869312805
Exacrs869312805
Varsomers869312805
Maprs869312805
PheGenIrs869312805
hapmaprs869312805
1000 genomesrs869312805
hgdprs869312805
ensemblrs869312805
gopubmedrs869312805
geneviewrs869312805
scholarrs869312805
googlers869312805
pharmgkbrs869312805
gwascentralrs869312805
openSNPrs869312805
23andMers869312805
23andMe allrs869312805
SNP Nexus

SNPshotrs869312805
SNPdbers869312805
MSV3drs869312805
GWAS Ctlgrs869312805
Max Magnitude0
ClinVar
Risk rs869312805(;)
Alt rs869312805(;)
Reference rs869312805(CCT;CCT)
Significance Probable-Pathogenic
Disease Fanconi anemia
Variation info
Gene FANCD2
CLNDBN Fanconi anemia, complementation group D2
Reversed 0
HGVS NC_000003.11:g.10106488_10106490delCCT
CLNSRC
CLNACC RCV000210268.1,