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rs886039304

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(CCATC;CCATC) 0 common in clinvar
Make rs886039304(-;-)
Make rs886039304(-;CCATC)
ReferenceGRCh38.p7 38.3/149
Chromosome17
Position19651767
GeneALDH3A2
is asnp
is mentioned by
dbSNPrs886039304
dbSNP (classic)rs886039304
ClinGenrs886039304
ebirs886039304
HLIrs886039304
Exacrs886039304
Gnomadrs886039304
Varsomers886039304
LitVarrs886039304
Maprs886039304
PheGenIrs886039304
Biobankrs886039304
1000 genomesrs886039304
hgdprs886039304
ensemblrs886039304
geneviewrs886039304
scholarrs886039304
googlers886039304
pharmgkbrs886039304
gwascentralrs886039304
openSNPrs886039304
23andMers886039304
SNPshotrs886039304
SNPdbers886039304
MSV3drs886039304
GWAS Ctlgrs886039304
Max Magnitude0
ClinVar
Risk rs886039304(-;-)
Alt rs886039304(-;-)
Reference Rs886039304(CCATC;CCATC)
Significance Pathogenic
Disease not provided
Variation info
Gene ALDH3A2
CLNDBN not provided
Reversed 0
HGVS NC_000017.10:g.19555080_19555084delCCATC
CLNSRC
CLNACC RCV000255939.1,