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rs750465793

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs750465793(G;T)
Make rs750465793(T;T)
ReferenceGRCh38.p2 38.2/144
Chromosome6
Position18122221
GeneNHLRC1
is asnp
is mentioned by
dbSNPrs750465793
ebirs750465793
HLIrs750465793
Exacrs750465793
Varsomers750465793
Maprs750465793
PheGenIrs750465793
hapmaprs750465793
1000 genomesrs750465793
hgdprs750465793
ensemblrs750465793
gopubmedrs750465793
geneviewrs750465793
scholarrs750465793
googlers750465793
pharmgkbrs750465793
gwascentralrs750465793
openSNPrs750465793
23andMers750465793
23andMe allrs750465793
SNP Nexus

SNPshotrs750465793
SNPdbers750465793
MSV3drs750465793
GWAS Ctlgrs750465793
Max Magnitude0
ClinVar
Risk rs750465793(T;T)
Alt rs750465793(T;T)
Reference rs750465793(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene NHLRC1
CLNDBN not provided
Reversed 0
HGVS NC_000006.11:g.18122452G>T
CLNSRC
CLNACC RCV000188211.1,