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rs1064793758

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(TTGT;TTGT) 0 common in clinvar
ChromosomeX
Position14845085
GeneFANCB
is asnp
is mentioned by
dbSNPrs1064793758
dbSNP (old)rs1064793758
ClinGenrs1064793758
ebirs1064793758
HLIrs1064793758
Exacrs1064793758
Gnomadrs1064793758
Varsomers1064793758
Maprs1064793758
PheGenIrs1064793758
Biobankrs1064793758
1000 genomesrs1064793758
hgdprs1064793758
ensemblrs1064793758
gopubmedrs1064793758
geneviewrs1064793758
scholarrs1064793758
googlers1064793758
pharmgkbrs1064793758
gwascentralrs1064793758
openSNPrs1064793758
23andMers1064793758
23andMe allrs1064793758
SNPshotrs1064793758
SNPdbers1064793758
MSV3drs1064793758
GWAS Ctlgrs1064793758
Max Magnitude0
ClinVar
Risk rs1064793758(-;-)
Alt rs1064793758(-;-)
Reference Rs1064793758(TTGT;TTGT)
Significance Pathogenic
Disease not provided
Variation info
Gene FANCB
CLNDBN not provided
Reversed 1
HGVS NC_000023.10:g.14863207_14863210delACAA
CLNSRC
CLNACC RCV000485610.1,