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rs796052758

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs796052758(-;-)
Make rs796052758(-;C)
ReferenceGRCh38.p2 38.2/146
Chromosome6
Position18122381
GeneNHLRC1
is asnp
is mentioned by
dbSNPrs796052758
ebirs796052758
HLIrs796052758
Exacrs796052758
Varsomers796052758
Maprs796052758
PheGenIrs796052758
hapmaprs796052758
1000 genomesrs796052758
hgdprs796052758
ensemblrs796052758
gopubmedrs796052758
geneviewrs796052758
scholarrs796052758
googlers796052758
pharmgkbrs796052758
gwascentralrs796052758
openSNPrs796052758
23andMers796052758
23andMe allrs796052758
SNP Nexus

SNPshotrs796052758
SNPdbers796052758
MSV3drs796052758
GWAS Ctlgrs796052758
Max Magnitude0
ClinVar
Risk rs796052758(;)
Alt rs796052758(;)
Reference rs796052758(C;C)
Significance Pathogenic
Disease not provided
Variation info
Gene NHLRC1
CLNDBN not provided
Reversed 1
HGVS NC_000006.11:g.18122612delG
CLNSRC
CLNACC RCV000188218.1,