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rs863224951

From SNPedia

Orientationplus
Geno Mag Summary
(-;-) 0 common in clinvar
Make rs863224951(-;GGCTAAAT)
Make rs863224951(GGCTAAAT;GGCTAAAT)
ReferenceGRCh38.p2 38.2/146
Chromosome12
Position8852231
GeneA2ML1
is asnp
is mentioned by
dbSNPrs863224951
ClinGenrs863224951
ebirs863224951
HLIrs863224951
Exacrs863224951
Varsomers863224951
Maprs863224951
PheGenIrs863224951
hapmaprs863224951
1000 genomesrs863224951
hgdprs863224951
ensemblrs863224951
gopubmedrs863224951
geneviewrs863224951
scholarrs863224951
googlers863224951
pharmgkbrs863224951
gwascentralrs863224951
openSNPrs863224951
23andMers863224951
23andMe allrs863224951
SNP Nexus

SNPshotrs863224951
SNPdbers863224951
MSV3drs863224951
GWAS Ctlgrs863224951
Max Magnitude0
ClinVar
Risk rs863224951(TGGCTAAA;TGGCTAAA)
Alt rs863224951(TGGCTAAA;TGGCTAAA)
Reference Rs863224951(;)
Significance Pathogenic
Disease Nonsyndromic otitis media
Variation info
Gene A2ML1
CLNDBN Nonsyndromic otitis media
Reversed 0
HGVS NC_000012.11:g.9004820_9004827dupGGCTAAAT
CLNSRC
CLNACC RCV000201239.1,