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rs137853155

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs137853155(A;A)
Make rs137853155(A;T)
ReferenceGRCh38 38.1/141
Chromosome20
Position10405465
GeneMKKS
is asnp
is mentioned by
dbSNPrs137853155
ebirs137853155
HLIrs137853155
Exacrs137853155
Varsomers137853155
Maprs137853155
PheGenIrs137853155
hapmaprs137853155
1000 genomesrs137853155
hgdprs137853155
ensemblrs137853155
gopubmedrs137853155
geneviewrs137853155
scholarrs137853155
googlers137853155
pharmgkbrs137853155
gwascentralrs137853155
openSNPrs137853155
23andMers137853155
23andMe allrs137853155
SNP Nexus

SNPshotrs137853155
SNPdbers137853155
MSV3drs137853155
GWAS Ctlgrs137853155
Max Magnitude0
OMIM604896
Desc
Variant0013
Relatedalso
ClinVar
Risk rs137853155(A;A)
Alt rs137853155(A;A)
Reference rs137853155(T;T)
Significance Untested
Disease Bardet-Biedl syndrome 6
Variation info
Gene MKKS
CLNDBN Bardet-Biedl syndrome 6
Reversed 1
HGVS NC_000020.10:g.10386113A>T
CLNSRC OMIM Allelic Variant
CLNACC SCV000025826.1, SCV000025826.1,