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rs796051978

From SNPedia

Orientationminus
Make rs796051978(-;-)
Make rs796051978(-;T)
ReferenceGRCh38.p2 38.2/147
Chromosome21
Position36756660
GeneHLCS
is asnp
is mentioned by
dbSNPrs796051978
ebirs796051978
HLIrs796051978
Exacrs796051978
Varsomers796051978
Maprs796051978
PheGenIrs796051978
hapmaprs796051978
1000 genomesrs796051978
hgdprs796051978
ensemblrs796051978
gopubmedrs796051978
geneviewrs796051978
scholarrs796051978
googlers796051978
pharmgkbrs796051978
gwascentralrs796051978
openSNPrs796051978
23andMers796051978
23andMe allrs796051978
SNP Nexus

SNPshotrs796051978
SNPdbers796051978
MSV3drs796051978
GWAS Ctlgrs796051978
Max Magnitude
ClinVar
Risk rs796051978(;)
Alt rs796051978(;)
Reference rs796051978(T;T)
Significance Pathogenic
Disease not provided
Variation info
Gene HLCS
CLNDBN not provided
Reversed 1
HGVS NC_000021.8:g.38128961delA
CLNSRC
CLNACC RCV000185967.1,