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rs1057518766

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs1057518766(A;A)
Make rs1057518766(A;G)
ReferenceGRCh38.p7 38.3/150
Chromosome21
Position45505372
GeneCOL18A1, SLC19A1
is asnp
is mentioned by
dbSNPrs1057518766
dbSNP (old)rs1057518766
ClinGenrs1057518766
ebirs1057518766
HLIrs1057518766
Exacrs1057518766
Gnomadrs1057518766
Varsomers1057518766
LitVarrs1057518766
Maprs1057518766
PheGenIrs1057518766
Biobankrs1057518766
1000 genomesrs1057518766
hgdprs1057518766
ensemblrs1057518766
gopubmedrs1057518766
geneviewrs1057518766
scholarrs1057518766
googlers1057518766
pharmgkbrs1057518766
gwascentralrs1057518766
openSNPrs1057518766
23andMers1057518766
23andMe allrs1057518766
SNPshotrs1057518766
SNPdbers1057518766
MSV3drs1057518766
GWAS Ctlgrs1057518766
Max Magnitude0
ClinVar
Risk rs1057518766(A;A)
Alt rs1057518766(A;A)
Reference Rs1057518766(G;G)
Significance Probable-Pathogenic
Disease Progressive neurodegenerative disease
Variation info
Gene COL18A1
CLNDBN Progressive neurodegenerative disease
Reversed 0
HGVS NC_000021.8:g.46925286G>A
CLNSRC
CLNACC RCV000415411.1,