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rs727503377

From SNPedia

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Geno Mag Summary
(CTGA;CTGA) 0 common in clinvar
Make rs727503377(-;-)
Make rs727503377(-;ACTG)
Make rs727503377(ACTG;ACTG)
ReferenceGRCh38.p2 38.2/144
ChromosomeX
Position83509410
is asnp
is mentioned by
dbSNPrs727503377
ebirs727503377
HLIrs727503377
Exacrs727503377
Varsomers727503377
Maprs727503377
PheGenIrs727503377
hapmaprs727503377
1000 genomesrs727503377
hgdprs727503377
ensemblrs727503377
gopubmedrs727503377
geneviewrs727503377
scholarrs727503377
googlers727503377
pharmgkbrs727503377
gwascentralrs727503377
openSNPrs727503377
23andMers727503377
23andMe allrs727503377
SNP Nexus

SNPshotrs727503377
SNPdbers727503377
MSV3drs727503377
GWAS Ctlgrs727503377
Max Magnitude0
ClinVar
Risk
Alt
Reference Rs727503377(CTGA;CTGA)
Significance Probable-Pathogenic
Disease Non-syndromic genetic deafness
Variation info
Gene
CLNDBN Non-syndromic genetic deafness
Reversed 0
HGVS NC_000023.10:g.82764418_82764421delACTG
CLNSRC
CLNACC RCV000151671.1,