Have questions? Visit https://www.reddit.com/r/SNPedia

rs373937326

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs373937326(A;A)
Make rs373937326(A;C)
ReferenceGRCh38.p2 38.2/144
Chromosome18
Position46534448
GeneLOXHD1
is asnp
is mentioned by
dbSNPrs373937326
ebirs373937326
HLIrs373937326
Exacrs373937326
Varsomers373937326
Maprs373937326
PheGenIrs373937326
hapmaprs373937326
1000 genomesrs373937326
hgdprs373937326
ensemblrs373937326
gopubmedrs373937326
geneviewrs373937326
scholarrs373937326
googlers373937326
pharmgkbrs373937326
gwascentralrs373937326
openSNPrs373937326
23andMers373937326
23andMe allrs373937326
SNP Nexus

SNPshotrs373937326
SNPdbers373937326
MSV3drs373937326
GWAS Ctlgrs373937326
Max Magnitude0
ClinVar
Risk rs373937326(A;A)
Alt rs373937326(A;A)
Reference rs373937326(C;C)
Significance Pathogenic
Disease Non-syndromic genetic deafness
Variation info
Gene LOXHD1
CLNDBN Non-syndromic genetic deafness
Reversed 0
HGVS NC_000018.9:g.44114411C>A
CLNSRC
CLNACC RCV000150972.1,