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rs200201752

From SNPedia

Orientationplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs200201752(C;C)
Make rs200201752(C;T)
ReferenceGRCh38.p2 38.2/144
Chromosome6
Position18121465
GeneNHLRC1
is asnp
is mentioned by
dbSNPrs200201752
ebirs200201752
HLIrs200201752
Exacrs200201752
Varsomers200201752
Maprs200201752
PheGenIrs200201752
hapmaprs200201752
1000 genomesrs200201752
hgdprs200201752
ensemblrs200201752
gopubmedrs200201752
geneviewrs200201752
scholarrs200201752
googlers200201752
pharmgkbrs200201752
gwascentralrs200201752
openSNPrs200201752
23andMers200201752
23andMe allrs200201752
SNP Nexus

SNPshotrs200201752
SNPdbers200201752
MSV3drs200201752
GWAS Ctlgrs200201752
Max Magnitude0
ClinVar
Risk rs200201752(C;C)
Alt rs200201752(C;C)
Reference rs200201752(T;T)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene NHLRC1
CLNDBN not provided
Reversed 0
HGVS NC_000006.11:g.18121696T>C
CLNSRC
CLNACC RCV000188216.1,