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rs137853187

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs137853187(A;A)
Make rs137853187(A;G)
ReferenceGRCh38 38.1/141
Chromosome11
Position72106180
GeneLRTOMT
is asnp
is mentioned by
dbSNPrs137853187
ebirs137853187
HLIrs137853187
Exacrs137853187
Varsomers137853187
Maprs137853187
PheGenIrs137853187
hapmaprs137853187
1000 genomesrs137853187
hgdprs137853187
ensemblrs137853187
gopubmedrs137853187
geneviewrs137853187
scholarrs137853187
googlers137853187
pharmgkbrs137853187
gwascentralrs137853187
openSNPrs137853187
23andMers137853187
23andMe allrs137853187
SNP Nexus

SNPshotrs137853187
SNPdbers137853187
MSV3drs137853187
GWAS Ctlgrs137853187
Max Magnitude0
OMIM612414
Desc
Variant0004
Relatedalso
ClinVar
Risk rs137853187(A;A)
Alt rs137853187(A;A)
Reference rs137853187(G;G)
Significance Pathogenic
Disease Deafness
Variation info
Gene LRTOMT
CLNDBN Deafness, autosomal recessive 63
Reversed 0
HGVS NC_000011.9:g.71817226G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000000575.2,