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rs387907178

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs387907178(C;C)
Make rs387907178(C;G)
ReferenceGRCh38 38.1/141
Chromosome1
Position109548838
GeneGNAI3
is asnp
is mentioned by
dbSNPrs387907178
ebirs387907178
HLIrs387907178
Exacrs387907178
Varsomers387907178
Maprs387907178
PheGenIrs387907178
hapmaprs387907178
1000 genomesrs387907178
hgdprs387907178
ensemblrs387907178
gopubmedrs387907178
geneviewrs387907178
scholarrs387907178
googlers387907178
pharmgkbrs387907178
gwascentralrs387907178
openSNPrs387907178
23andMers387907178
23andMe allrs387907178
SNP Nexus

SNPshotrs387907178
SNPdbers387907178
MSV3drs387907178
GWAS Ctlgrs387907178
Max Magnitude0
ClinVar
Risk rs387907178(C;C)
Alt rs387907178(C;C)
Reference rs387907178(G;G)
Significance Pathogenic
Disease Auriculocondylar syndrome 1
Variation info
Gene LOC101928560 GNAI3
CLNDBN Auriculocondylar syndrome 1
Reversed 0
HGVS NC_000001.10:g.110091460G>C
CLNSRC OMIM Allelic Variant
CLNACC RCV000024332.27,