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rs188119157

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs188119157(G;T)
Make rs188119157(T;T)
ReferenceGRCh38 38.1/141
Chromosome18
Position46563166
GeneLOXHD1
is asnp
is mentioned by
dbSNPrs188119157
ebirs188119157
HLIrs188119157
Exacrs188119157
Varsomers188119157
Maprs188119157
PheGenIrs188119157
hapmaprs188119157
1000 genomesrs188119157
hgdprs188119157
ensemblrs188119157
gopubmedrs188119157
geneviewrs188119157
scholarrs188119157
googlers188119157
pharmgkbrs188119157
gwascentralrs188119157
openSNPrs188119157
23andMers188119157
23andMe allrs188119157
SNP Nexus

SNPshotrs188119157
SNPdbers188119157
MSV3drs188119157
GWAS Ctlgrs188119157
Max Magnitude0
ClinVar
Risk rs188119157(A,T;A,T)
Alt rs188119157(A,T;A,T)
Reference rs188119157(G;G)
Significance Pathogenic
Disease Non-syndromic genetic deafness
Variation info
Gene LOXHD1
CLNDBN Non-syndromic genetic deafness
Reversed 0
HGVS NC_000018.9:g.44143129G>A
CLNSRC ClinVar
CLNACC RCV000041202.2,