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rs397514768

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs397514768(A;A)
Make rs397514768(A;C)
ReferenceGRCh38 38.1/141
Chromosome1
Position109573759
GeneGNAI3
is asnp
is mentioned by
dbSNPrs397514768
ebirs397514768
HLIrs397514768
Exacrs397514768
Varsomers397514768
Maprs397514768
PheGenIrs397514768
hapmaprs397514768
1000 genomesrs397514768
hgdprs397514768
ensemblrs397514768
gopubmedrs397514768
geneviewrs397514768
scholarrs397514768
googlers397514768
pharmgkbrs397514768
gwascentralrs397514768
openSNPrs397514768
23andMers397514768
23andMe allrs397514768
SNP Nexus

SNPshotrs397514768
SNPdbers397514768
MSV3drs397514768
GWAS Ctlgrs397514768
Max Magnitude0
ClinVar
Risk rs397514768(A;A)
Alt rs397514768(A;A)
Reference rs397514768(C;C)
Significance Pathogenic
Disease Auriculocondylar syndrome 1
Variation info
Gene GNAI3
CLNDBN Auriculocondylar syndrome 1
Reversed 0
HGVS NC_000001.10:g.110116381C>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000054837.26,