Have questions? Visit https://www.reddit.com/r/SNPedia

rs786204204

From SNPedia

Orientationminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs786204204(A;C)
Make rs786204204(C;C)
ReferenceGRCh38.p2 38.2/146
Chromosome16
Position89814517
GeneFANCA
is asnp
is mentioned by
dbSNPrs786204204
ebirs786204204
HLIrs786204204
Exacrs786204204
Varsomers786204204
Maprs786204204
PheGenIrs786204204
hapmaprs786204204
1000 genomesrs786204204
hgdprs786204204
ensemblrs786204204
gopubmedrs786204204
geneviewrs786204204
scholarrs786204204
googlers786204204
pharmgkbrs786204204
gwascentralrs786204204
openSNPrs786204204
23andMers786204204
23andMe allrs786204204
SNP Nexus

SNPshotrs786204204
SNPdbers786204204
MSV3drs786204204
GWAS Ctlgrs786204204
Max Magnitude0
ClinVar
Risk rs786204204(C;C)
Alt rs786204204(C;C)
Reference rs786204204(A;A)
Significance Pathogenic
Disease Fanconi anemia
Variation info
Gene FANCA
CLNDBN Fanconi anemia
Reversed 1
HGVS NC_000016.9:g.89880925T>G
CLNSRC
CLNACC RCV000168293.1,