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rs387906222

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs387906222(-;-)
Make rs387906222(-;G)
ReferenceGRCh38 38.1/141
Chromosome9
Position137199182
GeneTPRN
is asnp
is mentioned by
dbSNPrs387906222
ebirs387906222
HLIrs387906222
Exacrs387906222
Varsomers387906222
Maprs387906222
PheGenIrs387906222
hapmaprs387906222
1000 genomesrs387906222
hgdprs387906222
ensemblrs387906222
gopubmedrs387906222
geneviewrs387906222
scholarrs387906222
googlers387906222
pharmgkbrs387906222
gwascentralrs387906222
openSNPrs387906222
23andMers387906222
23andMe allrs387906222
SNP Nexus

SNPshotrs387906222
SNPdbers387906222
MSV3drs387906222
GWAS Ctlgrs387906222
Max Magnitude0
ClinVar
Risk rs387906222(;)
Alt rs387906222(;)
Reference rs387906222(G;G)
Significance Pathogenic
Disease Deafness
Variation info
Gene TPRN
CLNDBN Deafness, autosomal recessive 79
Reversed 1
HGVS NC_000009.11:g.140093634delC
CLNSRC OMIM Allelic Variant
CLNACC RCV000000161.3,