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rs72547573

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs72547573(C;T)
Make rs72547573(T;T)
ReferenceGRCh38.p7 38.3/150
Chromosome17
Position19663486
GeneALDH3A2
is asnp
is mentioned by
dbSNPrs72547573
dbSNP (classic)rs72547573
ClinGenrs72547573
ebirs72547573
HLIrs72547573
Exacrs72547573
Gnomadrs72547573
Varsomers72547573
LitVarrs72547573
Maprs72547573
PheGenIrs72547573
Biobankrs72547573
1000 genomesrs72547573
hgdprs72547573
ensemblrs72547573
geneviewrs72547573
scholarrs72547573
googlers72547573
pharmgkbrs72547573
gwascentralrs72547573
openSNPrs72547573
23andMers72547573
SNPshotrs72547573
SNPdbers72547573
MSV3drs72547573
GWAS Ctlgrs72547573
Max Magnitude0
ClinVar
Risk rs72547573(T;T)
Alt rs72547573(T;T)
Reference Rs72547573(C;C)
Significance Probable-Pathogenic
Disease Sjögren-Larsson syndrome
Variation info
Gene ALDH3A2
CLNDBN Sjögren-Larsson syndrome
Reversed 0
HGVS NC_000017.10:g.19566799C>T
CLNSRC
CLNACC RCV000410901.1,