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rs142365855

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs142365855(A;A)
Make rs142365855(A;G)
ReferenceGRCh38.p7 38.3/149
Chromosome3
Position10072982
GeneFANCD2
is asnp
is mentioned by
dbSNPrs142365855
dbSNP (old)rs142365855
ClinGenrs142365855
ebirs142365855
HLIrs142365855
Exacrs142365855
Gnomadrs142365855
Varsomers142365855
LitVarrs142365855
Maprs142365855
PheGenIrs142365855
Biobankrs142365855
1000 genomesrs142365855
hgdprs142365855
ensemblrs142365855
gopubmedrs142365855
geneviewrs142365855
scholarrs142365855
googlers142365855
pharmgkbrs142365855
gwascentralrs142365855
openSNPrs142365855
23andMers142365855
23andMe allrs142365855
SNPshotrs142365855
SNPdbers142365855
MSV3drs142365855
GWAS Ctlgrs142365855
Max Magnitude0
ClinVar
Risk rs142365855(A;A)
Alt rs142365855(A;A)
Reference Rs142365855(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene FANCD2
CLNDBN not provided
Reversed 0
HGVS NC_000003.11:g.10114666G>A
CLNSRC
CLNACC RCV000255506.1,