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rs587776861

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs587776861(A;A)
Make rs587776861(A;G)
ReferenceGRCh38 38.1/142
Chromosome4
Position73436100
GeneAFP
is asnp
is mentioned by
dbSNPrs587776861
ebirs587776861
HLIrs587776861
Exacrs587776861
Varsomers587776861
Maprs587776861
PheGenIrs587776861
hapmaprs587776861
1000 genomesrs587776861
hgdprs587776861
ensemblrs587776861
gopubmedrs587776861
geneviewrs587776861
scholarrs587776861
googlers587776861
pharmgkbrs587776861
gwascentralrs587776861
openSNPrs587776861
23andMers587776861
23andMe allrs587776861
SNP Nexus

SNPshotrs587776861
SNPdbers587776861
MSV3drs587776861
GWAS Ctlgrs587776861
Max Magnitude0
ClinVar
Risk rs587776861(A;A)
Alt rs587776861(A;A)
Reference rs587776861(G;G)
Significance Other
Disease Alpha-fetoprotein
Variation info
Gene AFP
CLNDBN Alpha-fetoprotein, hereditary persistence of
Reversed 0
HGVS NC_000004.11:g.74301817G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000019798.30,