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rs587776570

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
(TC;TC) 0 common in clinvar
Make rs587776570(-;-)
Make rs587776570(-;A)
ReferenceGRCh38 38.1/142
Chromosome16
Position89782879
GeneFANCA
is asnp
is mentioned by
dbSNPrs587776570
ebirs587776570
HLIrs587776570
Exacrs587776570
Varsomers587776570
Maprs587776570
PheGenIrs587776570
hapmaprs587776570
1000 genomesrs587776570
hgdprs587776570
ensemblrs587776570
gopubmedrs587776570
geneviewrs587776570
scholarrs587776570
googlers587776570
pharmgkbrs587776570
gwascentralrs587776570
openSNPrs587776570
23andMers587776570
23andMe allrs587776570
SNP Nexus

SNPshotrs587776570
SNPdbers587776570
MSV3drs587776570
GWAS Ctlgrs587776570
Max Magnitude0
ClinVar
Risk rs587776570(AC,C;AC,C)
Alt rs587776570(AC,C;AC,C)
Reference rs587776570(TC;TC)
Significance Pathogenic
Disease Fanconi anemia
Variation info
Gene FANCA
CLNDBN Fanconi anemia, complementation group A
Reversed 1
HGVS NC_000016.9:g.89849287delA
CLNSRC OMIM Allelic Variant
CLNACC RCV000003615.4,