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rs199621031

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs199621031(A;A)
Make rs199621031(A;G)
ReferenceGRCh38.p7 38.3/150
Chromosome17
Position18163251
GeneMYO15A
is asnp
is mentioned by
dbSNPrs199621031
dbSNP (old)rs199621031
ClinGenrs199621031
ebirs199621031
HLIrs199621031
Exacrs199621031
Gnomadrs199621031
Varsomers199621031
LitVarrs199621031
Maprs199621031
PheGenIrs199621031
Biobankrs199621031
1000 genomesrs199621031
hgdprs199621031
ensemblrs199621031
gopubmedrs199621031
geneviewrs199621031
scholarrs199621031
googlers199621031
pharmgkbrs199621031
gwascentralrs199621031
openSNPrs199621031
23andMers199621031
23andMe allrs199621031
SNPshotrs199621031
SNPdbers199621031
MSV3drs199621031
GWAS Ctlgrs199621031
Max Magnitude0
ClinVar
Risk rs199621031(A;A)
Alt rs199621031(A;A)
Reference Rs199621031(G;G)
Significance Probable-Pathogenic
Disease not specified Nonsyndromic Hearing Loss not provided
Variation info
Gene MYO15A
CLNDBN not specified Nonsyndromic Hearing Loss, Recessive not provided
Reversed 0
HGVS NC_000017.10:g.18066565G>A
CLNSRC
CLNACC RCV000217646.1, RCV000326631.1, RCV000413658.1,