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rs387907000

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs387907000(A;A)
Make rs387907000(A;G)
ReferenceGRCh38 38.1/141
Chromosome19
Position3590154
GeneGIPC3
is asnp
is mentioned by
dbSNPrs387907000
ebirs387907000
HLIrs387907000
Exacrs387907000
Varsomers387907000
Maprs387907000
PheGenIrs387907000
hapmaprs387907000
1000 genomesrs387907000
hgdprs387907000
ensemblrs387907000
gopubmedrs387907000
geneviewrs387907000
scholarrs387907000
googlers387907000
pharmgkbrs387907000
gwascentralrs387907000
openSNPrs387907000
23andMers387907000
23andMe allrs387907000
SNP Nexus

SNPshotrs387907000
SNPdbers387907000
MSV3drs387907000
GWAS Ctlgrs387907000
Max Magnitude0
ClinVar
Risk rs387907000(A;A)
Alt rs387907000(A;A)
Reference rs387907000(G;G)
Significance Pathogenic
Disease Deafness
Variation info
Gene GIPC3
CLNDBN Deafness, autosomal recessive 15
Reversed 0
HGVS NC_000019.9:g.3590152G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000023733.2,