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rs121912685

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs121912685(A;A)
Make rs121912685(A;G)
ReferenceGRCh38 38.1/141
Chromosome4
Position73442356
GeneAFP
is asnp
is mentioned by
dbSNPrs121912685
ebirs121912685
HLIrs121912685
Exacrs121912685
Varsomers121912685
Maprs121912685
PheGenIrs121912685
hapmaprs121912685
1000 genomesrs121912685
hgdprs121912685
ensemblrs121912685
gopubmedrs121912685
geneviewrs121912685
scholarrs121912685
googlers121912685
pharmgkbrs121912685
gwascentralrs121912685
openSNPrs121912685
23andMers121912685
23andMe allrs121912685
SNP Nexus

SNPshotrs121912685
SNPdbers121912685
MSV3drs121912685
GWAS Ctlgrs121912685
Max Magnitude0
OMIM104150
Desc
Variant0003
Relatedalso
ClinVar
Risk rs121912685(A;A)
Alt rs121912685(A;A)
Reference rs121912685(G;G)
Significance Pathogenic
Disease Alpha-fetoprotein deficiency
Variation info
Gene AFP
CLNDBN Alpha-fetoprotein deficiency
Reversed 0
HGVS NC_000004.11:g.74308073G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000019800.29,