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rs753824908

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs753824908(C;T)
Make rs753824908(T;T)
ReferenceGRCh38.p2 38.2/144
Chromosome21
Position45504431
GeneCOL18A1, SLC19A1
is asnp
is mentioned by
dbSNPrs753824908
ebirs753824908
HLIrs753824908
Exacrs753824908
Varsomers753824908
Maprs753824908
PheGenIrs753824908
hapmaprs753824908
1000 genomesrs753824908
hgdprs753824908
ensemblrs753824908
gopubmedrs753824908
geneviewrs753824908
scholarrs753824908
googlers753824908
pharmgkbrs753824908
gwascentralrs753824908
openSNPrs753824908
23andMers753824908
23andMe allrs753824908
SNP Nexus

SNPshotrs753824908
SNPdbers753824908
MSV3drs753824908
GWAS Ctlgrs753824908
Max Magnitude0
ClinVar
Risk rs753824908(T;T)
Alt rs753824908(T;T)
Reference rs753824908(C;C)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene LOC101928717 COL18A1
CLNDBN not provided
Reversed 0
HGVS NC_000021.8:g.46924345C>T
CLNSRC
CLNACC RCV000171509.1,