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rs281865467

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs281865467(C;T)
Make rs281865467(T;T)
ReferenceGRCh38.p7 38.3/150
Chromosome11
Position22259649
GeneANO5
is asnp
is mentioned by
dbSNPrs281865467
dbSNP (classic)rs281865467
ClinGenrs281865467
ebirs281865467
HLIrs281865467
Exacrs281865467
Gnomadrs281865467
Varsomers281865467
LitVarrs281865467
Maprs281865467
PheGenIrs281865467
Biobankrs281865467
1000 genomesrs281865467
hgdprs281865467
ensemblrs281865467
geneviewrs281865467
scholarrs281865467
googlers281865467
pharmgkbrs281865467
gwascentralrs281865467
openSNPrs281865467
23andMers281865467
23andMe allrs281865467
SNPshotrs281865467
SNPdbers281865467
MSV3drs281865467
GWAS Ctlgrs281865467
Max Magnitude0
ClinVar
Risk rs281865467(T;T)
Alt rs281865467(T;T)
Reference Rs281865467(C;C)
Significance Probable-Pathogenic
Disease not specified not provided
Variation info
Gene ANO5
CLNDBN not specified not provided
Reversed 0
HGVS NC_000011.9:g.22281195C>T
CLNSRC
CLNACC RCV000380299.1, RCV000487292.1,