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rs387907277

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs387907277(A;A)
Make rs387907277(A;G)
ReferenceGRCh38 38.1/141
Chromosome2
Position120984672
GeneGLI2
is asnp
is mentioned by
dbSNPrs387907277
ebirs387907277
HLIrs387907277
Exacrs387907277
Varsomers387907277
Maprs387907277
PheGenIrs387907277
hapmaprs387907277
1000 genomesrs387907277
hgdprs387907277
ensemblrs387907277
gopubmedrs387907277
geneviewrs387907277
scholarrs387907277
googlers387907277
pharmgkbrs387907277
gwascentralrs387907277
openSNPrs387907277
23andMers387907277
23andMe allrs387907277
SNP Nexus

SNPshotrs387907277
SNPdbers387907277
MSV3drs387907277
GWAS Ctlgrs387907277
Max Magnitude0
ClinVar
Risk rs387907277(A;A)
Alt rs387907277(A;A)
Reference rs387907277(G;G)
Significance Pathogenic
Disease Holoprosencephaly 9
Variation info
Gene GLI2
CLNDBN Holoprosencephaly 9
Reversed 0
HGVS NC_000002.11:g.121742248G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000030730.25,