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rs778507965

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs778507965(-;-)
Make rs778507965(-;C)
ReferenceGRCh38.p2 38.2/146
Chromosome16
Position89782870
GeneFANCA
is asnp
is mentioned by
dbSNPrs778507965
dbSNP (old)rs778507965
ClinGenrs778507965
ebirs778507965
HLIrs778507965
Exacrs778507965
Gnomadrs778507965
Varsomers778507965
Maprs778507965
PheGenIrs778507965
Biobankrs778507965
1000 genomesrs778507965
hgdprs778507965
ensemblrs778507965
gopubmedrs778507965
geneviewrs778507965
scholarrs778507965
googlers778507965
pharmgkbrs778507965
gwascentralrs778507965
openSNPrs778507965
23andMers778507965
23andMe allrs778507965
SNP Nexus

SNPshotrs778507965
SNPdbers778507965
MSV3drs778507965
GWAS Ctlgrs778507965
Max Magnitude0
ClinVar
Risk rs778507965(-;-)
Alt rs778507965(-;-)
Reference Rs778507965(C;C)
Significance Pathogenic
Disease Fanconi anemia
Variation info
Gene FANCA
CLNDBN Fanconi anemia, complementation group A
Reversed 0
HGVS NC_000016.9:g.89849278delC
CLNSRC OMIM Allelic Variant
CLNACC RCV000003612.3,