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rs149277003

From SNPedia

Orientationplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs149277003(C;C)
Make rs149277003(C;T)
ReferenceGRCh38.p2 38.2/146
Chromosome16
Position89746890
GeneFANCA
is asnp
is mentioned by
dbSNPrs149277003
ebirs149277003
HLIrs149277003
Exacrs149277003
Varsomers149277003
Maprs149277003
PheGenIrs149277003
hapmaprs149277003
1000 genomesrs149277003
hgdprs149277003
ensemblrs149277003
gopubmedrs149277003
geneviewrs149277003
scholarrs149277003
googlers149277003
pharmgkbrs149277003
gwascentralrs149277003
openSNPrs149277003
23andMers149277003
23andMe allrs149277003
SNP Nexus

SNPshotrs149277003
SNPdbers149277003
MSV3drs149277003
GWAS Ctlgrs149277003
Max Magnitude0
ClinVar
Risk rs149277003(C;C)
Alt rs149277003(C;C)
Reference rs149277003(T;T)
Significance Pathogenic
Disease Fanconi anemia
Variation info
Gene FANCA
CLNDBN Fanconi anemia
Reversed 0
HGVS NC_000016.9:g.89813298T>C
CLNSRC
CLNACC RCV000206698.2,