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rs747851434

From SNPedia

Orientationplus
Geno Mag Summary
(-;-) 0 common in clinvar
Make rs747851434(-;C)
Make rs747851434(C;C)
ReferenceGRCh38.p2 38.2/146
Chromosome16
Position89745026
GeneFANCA
is asnp
is mentioned by
dbSNPrs747851434
ClinGenrs747851434
ebirs747851434
HLIrs747851434
Exacrs747851434
Varsomers747851434
Maprs747851434
PheGenIrs747851434
hapmaprs747851434
1000 genomesrs747851434
hgdprs747851434
ensemblrs747851434
gopubmedrs747851434
geneviewrs747851434
scholarrs747851434
googlers747851434
pharmgkbrs747851434
gwascentralrs747851434
openSNPrs747851434
23andMers747851434
23andMe allrs747851434
SNP Nexus

SNPshotrs747851434
SNPdbers747851434
MSV3drs747851434
GWAS Ctlgrs747851434
Max Magnitude0
ClinVar
Risk rs747851434(C;C)
Alt rs747851434(C;C)
Reference Rs747851434(;)
Significance Pathogenic
Disease Fanconi anemia
Variation info
Gene FANCA
CLNDBN Fanconi anemia, complementation group A
Reversed 0
HGVS NC_000016.9:g.89811435dupC
CLNSRC OMIM Allelic Variant
CLNACC RCV000003613.3,