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rs886039325

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs886039325(C;C)
Make rs886039325(C;G)
ReferenceGRCh38.p7 38.3/149
Chromosome3
Position8745714
GeneCAV3, SSUH2
is asnp
is mentioned by
dbSNPrs886039325
dbSNP (classic)rs886039325
ClinGenrs886039325
ebirs886039325
HLIrs886039325
Exacrs886039325
Gnomadrs886039325
Varsomers886039325
LitVarrs886039325
Maprs886039325
PheGenIrs886039325
Biobankrs886039325
1000 genomesrs886039325
hgdprs886039325
ensemblrs886039325
geneviewrs886039325
scholarrs886039325
googlers886039325
pharmgkbrs886039325
gwascentralrs886039325
openSNPrs886039325
23andMers886039325
23andMe allrs886039325
SNPshotrs886039325
SNPdbers886039325
MSV3drs886039325
GWAS Ctlgrs886039325
Max Magnitude0
ClinVar
Risk rs886039325(C;C)
Alt rs886039325(C;C)
Reference Rs886039325(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene SSUH2 CAV3
CLNDBN not provided
Reversed 0
HGVS NC_000003.11:g.8787400G>C
CLNSRC
CLNACC RCV000256116.1,