Have questions? Visit https://www.reddit.com/r/SNPedia

rs371029653

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs371029653(A;A)
Make rs371029653(A;G)
ReferenceGRCh38.p2 38.2/146
Chromosome11
Position77179856
GeneMYO7A
is asnp
is mentioned by
dbSNPrs371029653
ebirs371029653
HLIrs371029653
Exacrs371029653
Varsomers371029653
Maprs371029653
PheGenIrs371029653
hapmaprs371029653
1000 genomesrs371029653
hgdprs371029653
ensemblrs371029653
gopubmedrs371029653
geneviewrs371029653
scholarrs371029653
googlers371029653
pharmgkbrs371029653
gwascentralrs371029653
openSNPrs371029653
23andMers371029653
23andMe allrs371029653
SNP Nexus

SNPshotrs371029653
SNPdbers371029653
MSV3drs371029653
GWAS Ctlgrs371029653
Max Magnitude0
ClinVar
Risk rs371029653(A;A)
Alt rs371029653(A;A)
Reference rs371029653(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene MYO7A
CLNDBN not provided
Reversed 0
HGVS NC_000011.9:g.76890902G>A
CLNSRC
CLNACC RCV000171199.1,