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rs770694933

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs770694933(-;-)
Make rs770694933(-;C)
ReferenceGRCh38.p7 38.3/149
Chromosome11
Position22276149
GeneANO5
is asnp
is mentioned by
dbSNPrs770694933
dbSNP (classic)rs770694933
ClinGenrs770694933
ebirs770694933
HLIrs770694933
Exacrs770694933
Gnomadrs770694933
Varsomers770694933
LitVarrs770694933
Maprs770694933
PheGenIrs770694933
Biobankrs770694933
1000 genomesrs770694933
hgdprs770694933
ensemblrs770694933
geneviewrs770694933
scholarrs770694933
googlers770694933
pharmgkbrs770694933
gwascentralrs770694933
openSNPrs770694933
23andMers770694933
23andMe allrs770694933
SNPshotrs770694933
SNPdbers770694933
MSV3drs770694933
GWAS Ctlgrs770694933
Max Magnitude0
ClinVar
Risk
Alt
Reference Rs770694933(C;C)
Significance Pathogenic
Disease not provided
Variation info
Gene ANO5
CLNDBN not provided
Reversed 0
HGVS NC_000011.9:g.22297695delC
CLNSRC
CLNACC RCV000313812.1,