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rs549138385

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs549138385(C;T)
Make rs549138385(T;T)
ReferenceGRCh38.p7 38.3/150
Chromosome17
Position18135747
GeneMYO15A
is asnp
is mentioned by
dbSNPrs549138385
dbSNP (classic)rs549138385
ClinGenrs549138385
ebirs549138385
HLIrs549138385
Exacrs549138385
Gnomadrs549138385
Varsomers549138385
LitVarrs549138385
Maprs549138385
PheGenIrs549138385
Biobankrs549138385
1000 genomesrs549138385
hgdprs549138385
ensemblrs549138385
geneviewrs549138385
scholarrs549138385
googlers549138385
pharmgkbrs549138385
gwascentralrs549138385
openSNPrs549138385
23andMers549138385
SNPshotrs549138385
SNPdbers549138385
MSV3drs549138385
GWAS Ctlgrs549138385
Max Magnitude0
ClinVar
Risk rs549138385(G;G) rs549138385(T;T)
Alt rs549138385(G;G) rs549138385(T;T)
Reference Rs549138385(C;C)
Significance Pathogenic
Disease not provided
Variation info
Gene MYO15A
CLNDBN not provided
Reversed 0
HGVS NC_000017.10:g.18039061C>T
CLNSRC
CLNACC RCV000483838.1,