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rs755572135

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs755572135(A;A)
Make rs755572135(A;G)
ReferenceGRCh38.p2 38.2/147
Chromosome17
Position17798202
GeneRAI1
is asnp
is mentioned by
dbSNPrs755572135
ClinGenrs755572135
ebirs755572135
HLIrs755572135
Exacrs755572135
Varsomers755572135
Maprs755572135
PheGenIrs755572135
hapmaprs755572135
1000 genomesrs755572135
hgdprs755572135
ensemblrs755572135
gopubmedrs755572135
geneviewrs755572135
scholarrs755572135
googlers755572135
pharmgkbrs755572135
gwascentralrs755572135
openSNPrs755572135
23andMers755572135
23andMe allrs755572135
SNP Nexus

SNPshotrs755572135
SNPdbers755572135
MSV3drs755572135
GWAS Ctlgrs755572135
Max Magnitude0
ClinVar
Risk rs755572135(A;A)
Alt rs755572135(A;A)
Reference Rs755572135(G;G)
Significance Pathogenic
Disease not specified Deafness
Variation info
Gene RAI1
CLNDBN not specified Deafness, autosomal recessive 9
Reversed 0
HGVS NC_000017.10:g.17701516G>A
CLNSRC
CLNACC RCV000194060.1, RCV000239360.1,