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rs767271426

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs767271426(-;-)
Make rs767271426(-;G)
ReferenceGRCh38.p2 38.2/147
Chromosome1
Position16053708
GeneCLCNKB
is asnp
is mentioned by
dbSNPrs767271426
ebirs767271426
HLIrs767271426
Exacrs767271426
Varsomers767271426
Maprs767271426
PheGenIrs767271426
hapmaprs767271426
1000 genomesrs767271426
hgdprs767271426
ensemblrs767271426
gopubmedrs767271426
geneviewrs767271426
scholarrs767271426
googlers767271426
pharmgkbrs767271426
gwascentralrs767271426
openSNPrs767271426
23andMers767271426
23andMe allrs767271426
SNP Nexus

SNPshotrs767271426
SNPdbers767271426
MSV3drs767271426
GWAS Ctlgrs767271426
Max Magnitude0
ClinVar
Risk rs767271426(;)
Alt rs767271426(;)
Reference rs767271426(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene CLCNKB
CLNDBN not provided
Reversed 0
HGVS NC_000001.10:g.16380203delG
CLNSRC
CLNACC RCV000224201.1,