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rs1057521855

From SNPedia
Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs1057521855(C;T)
Make rs1057521855(T;T)
ReferenceGRCh38.p7 38.3/150
Chromosome16
Position89783084
GeneFANCA
is asnp
is mentioned by
dbSNPrs1057521855
dbSNP (old)rs1057521855
ClinGenrs1057521855
ebirs1057521855
HLIrs1057521855
Exacrs1057521855
Gnomadrs1057521855
Varsomers1057521855
Maprs1057521855
PheGenIrs1057521855
Biobankrs1057521855
1000 genomesrs1057521855
hgdprs1057521855
ensemblrs1057521855
gopubmedrs1057521855
geneviewrs1057521855
scholarrs1057521855
googlers1057521855
pharmgkbrs1057521855
gwascentralrs1057521855
openSNPrs1057521855
23andMers1057521855
23andMe allrs1057521855
SNPshotrs1057521855
SNPdbers1057521855
MSV3drs1057521855
GWAS Ctlgrs1057521855
Max Magnitude0
ClinVar
Risk rs1057521855(T;T)
Alt rs1057521855(T;T)
Reference Rs1057521855(C;C)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene FANCA
CLNDBN not provided
Reversed 1
HGVS NC_000016.9:g.89849492G>A
CLNSRC
CLNACC RCV000432541.1,