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rs796051977

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs796051977(C;T)
Make rs796051977(T;T)
ReferenceGRCh38.p2 38.2/147
Chromosome21
Position36937222
GeneHLCS
is asnp
is mentioned by
dbSNPrs796051977
ebirs796051977
HLIrs796051977
Exacrs796051977
Varsomers796051977
Maprs796051977
PheGenIrs796051977
hapmaprs796051977
1000 genomesrs796051977
hgdprs796051977
ensemblrs796051977
gopubmedrs796051977
geneviewrs796051977
scholarrs796051977
googlers796051977
pharmgkbrs796051977
gwascentralrs796051977
openSNPrs796051977
23andMers796051977
23andMe allrs796051977
SNP Nexus

SNPshotrs796051977
SNPdbers796051977
MSV3drs796051977
GWAS Ctlgrs796051977
Max Magnitude0
ClinVar
Risk rs796051977(T;T)
Alt rs796051977(T;T)
Reference rs796051977(C;C)
Significance Pathogenic
Disease not provided
Variation info
Gene HLCS
CLNDBN not provided
Reversed 1
HGVS NC_000021.8:g.38309522G>A
CLNSRC
CLNACC RCV000185965.1,