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rs786205554

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs786205554(C;T)
Make rs786205554(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome21
Position45493561
GeneCOL18A1
is asnp
is mentioned by
dbSNPrs786205554
ebirs786205554
HLIrs786205554
Exacrs786205554
Varsomers786205554
Maprs786205554
PheGenIrs786205554
hapmaprs786205554
1000 genomesrs786205554
hgdprs786205554
ensemblrs786205554
gopubmedrs786205554
geneviewrs786205554
scholarrs786205554
googlers786205554
pharmgkbrs786205554
gwascentralrs786205554
openSNPrs786205554
23andMers786205554
23andMe allrs786205554
SNP Nexus

SNPshotrs786205554
SNPdbers786205554
MSV3drs786205554
GWAS Ctlgrs786205554
Max Magnitude0
ClinVar
Risk rs786205554(T;T)
Alt rs786205554(T;T)
Reference rs786205554(C;C)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene COL18A1
CLNDBN not provided
Reversed 0
HGVS NC_000021.8:g.46913475C>T
CLNSRC
CLNACC RCV000171350.1,