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rs17233141

From SNPedia

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Geno Mag Summary
(G;G) 0 common in clinvar
Make rs17233141(C;C)
Make rs17233141(C;G)
ReferenceGRCh38.p2 38.2/146
Chromosome16
Position89767168
GeneFANCA
is asnp
is mentioned by
dbSNPrs17233141
ebirs17233141
HLIrs17233141
Exacrs17233141
Varsomers17233141
Maprs17233141
PheGenIrs17233141
hapmaprs17233141
1000 genomesrs17233141
hgdprs17233141
ensemblrs17233141
gopubmedrs17233141
geneviewrs17233141
scholarrs17233141
googlers17233141
pharmgkbrs17233141
gwascentralrs17233141
openSNPrs17233141
23andMers17233141
23andMe allrs17233141
SNP Nexus

SNPshotrs17233141
SNPdbers17233141
MSV3drs17233141
GWAS Ctlgrs17233141
Max Magnitude0
ClinVar
Risk rs17233141(C;C)
Alt rs17233141(C;C)
Reference rs17233141(G;G)
Significance Pathogenic
Disease not specified Fanconi anemia Fanconi anemia
Variation info
Gene FANCA
CLNDBN not specified Fanconi anemia, complementation group A Fanconi anemia
Reversed 0
HGVS NC_000016.9:g.89833576G>C
CLNSRC
CLNACC RCV000120929.1, RCV000202580.1, RCV000206151.2,