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rs780825099

From SNPedia

Orientationplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs780825099(G;G)
Make rs780825099(G;T)
ReferenceGRCh38.p2 38.2/146
Chromosome16
Position89765062
GeneFANCA
is asnp
is mentioned by
dbSNPrs780825099
ebirs780825099
HLIrs780825099
Exacrs780825099
Varsomers780825099
Maprs780825099
PheGenIrs780825099
hapmaprs780825099
1000 genomesrs780825099
hgdprs780825099
ensemblrs780825099
gopubmedrs780825099
geneviewrs780825099
scholarrs780825099
googlers780825099
pharmgkbrs780825099
gwascentralrs780825099
openSNPrs780825099
23andMers780825099
23andMe allrs780825099
SNP Nexus

SNPshotrs780825099
SNPdbers780825099
MSV3drs780825099
GWAS Ctlgrs780825099
Max Magnitude0
ClinVar
Risk rs780825099(G;G)
Alt rs780825099(G;G)
Reference rs780825099(T;T)
Significance Probable-Pathogenic
Disease Fanconi anemia
Variation info
Gene FANCA
CLNDBN Fanconi anemia
Reversed 0
HGVS NC_000016.9:g.89831470T>G
CLNSRC
CLNACC RCV000199923.1,