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rs759217526

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(-;-) 0 common in clinvar
Make rs759217526(-;TAAT)
Make rs759217526(TAAT;TAAT)
ReferenceGRCh38.p2 38.2/146
Chromosome2
Position58159793
GeneFANCL, VRK2
is asnp
is mentioned by
dbSNPrs759217526
ClinGenrs759217526
ebirs759217526
HLIrs759217526
Exacrs759217526
Varsomers759217526
Maprs759217526
PheGenIrs759217526
hapmaprs759217526
1000 genomesrs759217526
hgdprs759217526
ensemblrs759217526
gopubmedrs759217526
geneviewrs759217526
scholarrs759217526
googlers759217526
pharmgkbrs759217526
gwascentralrs759217526
openSNPrs759217526
23andMers759217526
23andMe allrs759217526
SNP Nexus

SNPshotrs759217526
SNPdbers759217526
MSV3drs759217526
GWAS Ctlgrs759217526
Max Magnitude0
ClinVar
Risk rs759217526(TAAT;TAAT)
Alt rs759217526(TAAT;TAAT)
Reference Rs759217526(-;-)
Significance Other
Disease Fanconi anemia Fanconi anemia
Variation info
Gene VRK2 FANCL
CLNDBN Fanconi anemia, complementation group L Fanconi anemia
Reversed 0
HGVS NC_000002.11:g.58386929_58386932dupTAAT
CLNSRC
CLNACC RCV000192919.2, RCV000226300.3,