Have questions? Visit https://www.reddit.com/r/SNPedia

rs121917707

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs121917707(A;A)
Make rs121917707(A;G)
ReferenceGRCh38 38.1/141
Chromosome2
Position120975064
GeneGLI2
is asnp
is mentioned by
dbSNPrs121917707
ebirs121917707
HLIrs121917707
Exacrs121917707
Varsomers121917707
Maprs121917707
PheGenIrs121917707
hapmaprs121917707
1000 genomesrs121917707
hgdprs121917707
ensemblrs121917707
gopubmedrs121917707
geneviewrs121917707
scholarrs121917707
googlers121917707
pharmgkbrs121917707
gwascentralrs121917707
openSNPrs121917707
23andMers121917707
23andMe allrs121917707
SNP Nexus

SNPshotrs121917707
SNPdbers121917707
MSV3drs121917707
GWAS Ctlgrs121917707
Max Magnitude0
OMIM165230
Desc
Variant0002
Relatedalso
ClinVar
Risk rs121917707(A;A)
Alt rs121917707(A;A)
Reference rs121917707(G;G)
Significance Pathogenic
Disease Holoprosencephaly 9
Variation info
Gene GLI2
CLNDBN Holoprosencephaly 9
Reversed 0
HGVS NC_000002.11:g.121732640G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000014847.26,