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rs201824235

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs201824235(A;T)
Make rs201824235(T;T)
ReferenceGRCh38 38.1/142
Chromosome4
Position42963153
GeneGRXCR1
is asnp
is mentioned by
dbSNPrs201824235
ebirs201824235
HLIrs201824235
Exacrs201824235
Varsomers201824235
Maprs201824235
PheGenIrs201824235
hapmaprs201824235
1000 genomesrs201824235
hgdprs201824235
ensemblrs201824235
gopubmedrs201824235
geneviewrs201824235
scholarrs201824235
googlers201824235
pharmgkbrs201824235
gwascentralrs201824235
openSNPrs201824235
23andMers201824235
23andMe allrs201824235
SNP Nexus

SNPshotrs201824235
SNPdbers201824235
MSV3drs201824235
GWAS Ctlgrs201824235
Max Magnitude0
ClinVar
Risk rs201824235(T;T)
Alt rs201824235(T;T)
Reference rs201824235(A;A)
Significance Pathogenic
Disease Deafness
Variation info
Gene GRXCR1
CLNDBN Deafness, autosomal recessive 25
Reversed 0
HGVS NC_000004.11:g.42965170A>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000000217.2,