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rs281797259

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs281797259(C;G)
Make rs281797259(G;G)
ReferenceGRCh38 38.1/141
Chromosome20
Position10405464
GeneMKKS
is asnp
is mentioned by
dbSNPrs281797259
ebirs281797259
HLIrs281797259
Exacrs281797259
Varsomers281797259
Maprs281797259
PheGenIrs281797259
hapmaprs281797259
1000 genomesrs281797259
hgdprs281797259
ensemblrs281797259
gopubmedrs281797259
geneviewrs281797259
scholarrs281797259
googlers281797259
pharmgkbrs281797259
gwascentralrs281797259
openSNPrs281797259
23andMers281797259
23andMe allrs281797259
SNP Nexus

SNPshotrs281797259
SNPdbers281797259
MSV3drs281797259
GWAS Ctlgrs281797259
Max Magnitude0
ClinVar
Risk rs281797259(G;G)
Alt rs281797259(G;G)
Reference rs281797259(C;C)
Significance Pathogenic
Disease Bardet-biedl syndrome 2/6
Variation info
Gene MKKS
CLNDBN Bardet-biedl syndrome 2/6, digenic
Reversed 0
HGVS NC_000020.10:g.10386112C>G
CLNSRC OMIM Allelic Variant
CLNACC RCV000005644.3,