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rs547918064

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs547918064(C;C)
Make rs547918064(C;G)
ReferenceGRCh38.p7 38.3/150
Chromosome15
Position100898147
GeneALDH1A3, LOC101927751
is asnp
is mentioned by
dbSNPrs547918064
dbSNP (classic)rs547918064
ClinGenrs547918064
ebirs547918064
HLIrs547918064
Exacrs547918064
Gnomadrs547918064
Varsomers547918064
LitVarrs547918064
Maprs547918064
PheGenIrs547918064
Biobankrs547918064
1000 genomesrs547918064
hgdprs547918064
ensemblrs547918064
geneviewrs547918064
scholarrs547918064
googlers547918064
pharmgkbrs547918064
gwascentralrs547918064
openSNPrs547918064
23andMers547918064
23andMe allrs547918064
SNPshotrs547918064
SNPdbers547918064
MSV3drs547918064
GWAS Ctlgrs547918064
Max Magnitude0
ClinVar
Risk rs547918064(C;C) rs547918064(T;T)
Alt rs547918064(C;C) rs547918064(T;T)
Reference Rs547918064(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene LOC101927751 ALDH1A3
CLNDBN not provided
Reversed 0
HGVS NC_000015.9:g.101438352G>A
CLNSRC
CLNACC RCV000493670.1,