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rs121917881

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs121917881(A;A)
Make rs121917881(A;G)
ReferenceGRCh38 38.1/141
Chromosome2
Position44942310
GeneSIX3
is asnp
is mentioned by
dbSNPrs121917881
ebirs121917881
HLIrs121917881
Exacrs121917881
Varsomers121917881
Maprs121917881
PheGenIrs121917881
hapmaprs121917881
1000 genomesrs121917881
hgdprs121917881
ensemblrs121917881
gopubmedrs121917881
geneviewrs121917881
scholarrs121917881
googlers121917881
pharmgkbrs121917881
gwascentralrs121917881
openSNPrs121917881
23andMers121917881
23andMe allrs121917881
SNP Nexus

SNPshotrs121917881
SNPdbers121917881
MSV3drs121917881
GWAS Ctlgrs121917881
Max Magnitude0
ClinVar
Risk rs121917881(A;A)
Alt rs121917881(A;A)
Reference rs121917881(G;G)
Significance Pathogenic
Disease Holoprosencephaly 2
Variation info
Gene SIX3 SIX3-AS1
CLNDBN Holoprosencephaly 2
Reversed 0
HGVS NC_000002.11:g.45169449G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000006471.2,