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rs529961953

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs529961953(A;A)
Make rs529961953(A;C)
ReferenceGRCh38.p7 38.3/150
Chromosome11
Position22257738
GeneANO5
is asnp
is mentioned by
dbSNPrs529961953
dbSNP (classic)rs529961953
ClinGenrs529961953
ebirs529961953
HLIrs529961953
Exacrs529961953
Gnomadrs529961953
Varsomers529961953
LitVarrs529961953
Maprs529961953
PheGenIrs529961953
Biobankrs529961953
1000 genomesrs529961953
hgdprs529961953
ensemblrs529961953
geneviewrs529961953
scholarrs529961953
googlers529961953
pharmgkbrs529961953
gwascentralrs529961953
openSNPrs529961953
23andMers529961953
23andMe allrs529961953
SNPshotrs529961953
SNPdbers529961953
MSV3drs529961953
GWAS Ctlgrs529961953
Max Magnitude0
ClinVar
Risk rs529961953(A;A)
Alt rs529961953(A;A)
Reference Rs529961953(C;C)
Significance Pathogenic
Disease not provided
Variation info
Gene ANO5
CLNDBN not provided
Reversed 0
HGVS NC_000011.9:g.22279284C>A
CLNSRC
CLNACC RCV000438945.1,