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rs878852989

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs878852989(C;T)
Make rs878852989(T;T)
ReferenceGRCh38.p2 38.2/147
Chromosome21
Position36756546
GeneHLCS
is asnp
is mentioned by
dbSNPrs878852989
ebirs878852989
HLIrs878852989
Exacrs878852989
Varsomers878852989
Maprs878852989
PheGenIrs878852989
hapmaprs878852989
1000 genomesrs878852989
hgdprs878852989
ensemblrs878852989
gopubmedrs878852989
geneviewrs878852989
scholarrs878852989
googlers878852989
pharmgkbrs878852989
gwascentralrs878852989
openSNPrs878852989
23andMers878852989
23andMe allrs878852989
SNP Nexus

SNPshotrs878852989
SNPdbers878852989
MSV3drs878852989
GWAS Ctlgrs878852989
Max Magnitude0
ClinVar
Risk rs878852989(T;T)
Alt rs878852989(T;T)
Reference rs878852989(C;C)
Significance Pathogenic
Disease not provided
Variation info
Gene HLCS
CLNDBN not provided
Reversed 1
HGVS NC_000021.8:g.38128847G>A
CLNSRC
CLNACC RCV000224257.1,