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rs397517865

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs397517865(C;C)
Make rs397517865(C;G)
ReferenceGRCh38 38.1/141
Chromosome3
Position46705910
GeneTMIE
is asnp
is mentioned by
dbSNPrs397517865
ebirs397517865
HLIrs397517865
Exacrs397517865
Varsomers397517865
Maprs397517865
PheGenIrs397517865
hapmaprs397517865
1000 genomesrs397517865
hgdprs397517865
ensemblrs397517865
gopubmedrs397517865
geneviewrs397517865
scholarrs397517865
googlers397517865
pharmgkbrs397517865
gwascentralrs397517865
openSNPrs397517865
23andMers397517865
23andMe allrs397517865
SNP Nexus

SNPshotrs397517865
SNPdbers397517865
MSV3drs397517865
GWAS Ctlgrs397517865
Max Magnitude0
ClinVar
Risk rs397517865(A,C;A,C)
Alt rs397517865(A,C;A,C)
Reference rs397517865(G;G)
Significance Probable-Pathogenic
Disease Non-syndromic genetic deafness
Variation info
Gene TMIE
CLNDBN Non-syndromic genetic deafness
Reversed 0
HGVS NC_000003.11:g.46747400G>C
CLNSRC ClinVar
CLNACC RCV000041229.2,