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rs587777424

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(;) 0 common in clinvar
Make rs587777424(-;-)
Make rs587777424(-;A)
Make rs587777424(A;A)
ReferenceGRCh38 38.1/142
Chromosome5
Position145859766
GeneGRXCR2
is asnp
is mentioned by
dbSNPrs587777424
ebirs587777424
HLIrs587777424
Exacrs587777424
Varsomers587777424
Maprs587777424
PheGenIrs587777424
hapmaprs587777424
1000 genomesrs587777424
hgdprs587777424
ensemblrs587777424
gopubmedrs587777424
geneviewrs587777424
scholarrs587777424
googlers587777424
pharmgkbrs587777424
gwascentralrs587777424
openSNPrs587777424
23andMers587777424
23andMe allrs587777424
SNP Nexus

SNPshotrs587777424
SNPdbers587777424
MSV3drs587777424
GWAS Ctlgrs587777424
Max Magnitude0
ClinVar
Risk rs587777424(A;A)
Alt rs587777424(A;A)
Reference rs587777424(;)
Significance Pathogenic
Disease Deafness
Variation info
Gene GRXCR2
CLNDBN Deafness, autosomal recessive 101
Reversed 0
HGVS NC_000005.9:g.145239329dupA
CLNSRC OMIM Allelic Variant
CLNACC RCV000119847.2,