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rs727503315

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs727503315(-;-)
Make rs727503315(-;C)
ReferenceGRCh38.p2 38.2/144
Chromosome17
Position18150442
GeneLOC105371568, MYO15A
is asnp
is mentioned by
dbSNPrs727503315
ebirs727503315
HLIrs727503315
Exacrs727503315
Varsomers727503315
Maprs727503315
PheGenIrs727503315
hapmaprs727503315
1000 genomesrs727503315
hgdprs727503315
ensemblrs727503315
gopubmedrs727503315
geneviewrs727503315
scholarrs727503315
googlers727503315
pharmgkbrs727503315
gwascentralrs727503315
openSNPrs727503315
23andMers727503315
23andMe allrs727503315
SNP Nexus

SNPshotrs727503315
SNPdbers727503315
MSV3drs727503315
GWAS Ctlgrs727503315
Max Magnitude0
ClinVar
Risk rs727503315(;)
Alt rs727503315(;)
Reference rs727503315(C;C)
Significance Pathogenic
Disease Non-syndromic genetic deafness
Variation info
Gene MYO15A
CLNDBN Non-syndromic genetic deafness
Reversed 0
HGVS NC_000017.10:g.18053756delC
CLNSRC
CLNACC RCV000151407.1,