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rs1010078101

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs1010078101(A;A)
Make rs1010078101(A;G)
ReferenceGRCh38.p7 38.3/150
Chromosome17
Position19665042
GeneALDH3A2
is asnp
is mentioned by
dbSNPrs1010078101
dbSNP (old)rs1010078101
ClinGenrs1010078101
ebirs1010078101
HLIrs1010078101
Exacrs1010078101
Gnomadrs1010078101
Varsomers1010078101
LitVarrs1010078101
Maprs1010078101
PheGenIrs1010078101
Biobankrs1010078101
1000 genomesrs1010078101
hgdprs1010078101
ensemblrs1010078101
gopubmedrs1010078101
geneviewrs1010078101
scholarrs1010078101
googlers1010078101
pharmgkbrs1010078101
gwascentralrs1010078101
openSNPrs1010078101
23andMers1010078101
23andMe allrs1010078101
SNPshotrs1010078101
SNPdbers1010078101
MSV3drs1010078101
GWAS Ctlgrs1010078101
Max Magnitude0
ClinVar
Risk rs1010078101(A;A)
Alt rs1010078101(A;A)
Reference Rs1010078101(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene ALDH3A2
CLNDBN not provided
Reversed 0
HGVS NC_000017.10:g.19568355G>A
CLNSRC
CLNACC RCV000437687.1,