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rs786205631

From SNPedia

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Geno Mag Summary
(G;G) 0 common in clinvar
Make rs786205631(C;C)
Make rs786205631(C;G)
ReferenceGRCh38.p2 38.2/146
Chromosome2
Position3603614
GeneCOLEC11
is asnp
is mentioned by
dbSNPrs786205631
ebirs786205631
HLIrs786205631
Exacrs786205631
Varsomers786205631
Maprs786205631
PheGenIrs786205631
hapmaprs786205631
1000 genomesrs786205631
hgdprs786205631
ensemblrs786205631
gopubmedrs786205631
geneviewrs786205631
scholarrs786205631
googlers786205631
pharmgkbrs786205631
gwascentralrs786205631
openSNPrs786205631
23andMers786205631
23andMe allrs786205631
SNP Nexus

SNPshotrs786205631
SNPdbers786205631
MSV3drs786205631
GWAS Ctlgrs786205631
Max Magnitude0
ClinVar
Risk rs786205631(C;C)
Alt rs786205631(C;C)
Reference rs786205631(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene COLEC11
CLNDBN not provided
Reversed 0
HGVS NC_000002.11:g.3651204G>C
CLNSRC
CLNACC RCV000171491.1,