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rs786204246

From SNPedia

Orientationminus
Geno Mag Summary
(TTC;TTC) 0 common in clinvar
Make rs786204246(-;-)
Make rs786204246(-;TTC)
ReferenceGRCh38.p2 38.2/146
Chromosome16
Position89746834
GeneFANCA
is asnp
is mentioned by
dbSNPrs786204246
ebirs786204246
HLIrs786204246
Exacrs786204246
Varsomers786204246
Maprs786204246
PheGenIrs786204246
hapmaprs786204246
1000 genomesrs786204246
hgdprs786204246
ensemblrs786204246
gopubmedrs786204246
geneviewrs786204246
scholarrs786204246
googlers786204246
pharmgkbrs786204246
gwascentralrs786204246
openSNPrs786204246
23andMers786204246
23andMe allrs786204246
SNP Nexus

SNPshotrs786204246
SNPdbers786204246
MSV3drs786204246
GWAS Ctlgrs786204246
Max Magnitude0
ClinVar
Risk rs786204246(;)
Alt rs786204246(;)
Reference rs786204246(TTC;TTC)
Significance Pathogenic
Disease Fanconi anemia
Variation info
Gene FANCA
CLNDBN Fanconi anemia
Reversed 1
HGVS NC_000016.9:g.89813242_89813244delGAA
CLNSRC
CLNACC RCV000168439.2,