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rs587783028

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs587783028(G;T)
Make rs587783028(T;T)
ReferenceGRCh38.p2 38.2/144
Chromosome16
Position89752137
GeneFANCA
is asnp
is mentioned by
dbSNPrs587783028
ebirs587783028
HLIrs587783028
Exacrs587783028
Varsomers587783028
Maprs587783028
PheGenIrs587783028
hapmaprs587783028
1000 genomesrs587783028
hgdprs587783028
ensemblrs587783028
gopubmedrs587783028
geneviewrs587783028
scholarrs587783028
googlers587783028
pharmgkbrs587783028
gwascentralrs587783028
openSNPrs587783028
23andMers587783028
23andMe allrs587783028
SNP Nexus

SNPshotrs587783028
SNPdbers587783028
MSV3drs587783028
GWAS Ctlgrs587783028
Max Magnitude0
ClinVar
Risk rs587783028(A,T;A,T)
Alt rs587783028(A,T;A,T)
Reference rs587783028(G;G)
Significance Pathogenic
Disease Fanconi anemia
Variation info
Gene FANCA
CLNDBN Fanconi anemia, complementation group A
Reversed 1
HGVS NC_000016.9:g.89818545C>A
CLNSRC
CLNACC RCV000144483.1,