Have questions? Visit https://www.reddit.com/r/SNPedia

rs786205508

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs786205508(C;T)
Make rs786205508(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome17
Position58208542
GeneMKS1
is asnp
is mentioned by
dbSNPrs786205508
ebirs786205508
HLIrs786205508
Exacrs786205508
Varsomers786205508
Maprs786205508
PheGenIrs786205508
hapmaprs786205508
1000 genomesrs786205508
hgdprs786205508
ensemblrs786205508
gopubmedrs786205508
geneviewrs786205508
scholarrs786205508
googlers786205508
pharmgkbrs786205508
gwascentralrs786205508
openSNPrs786205508
23andMers786205508
23andMe allrs786205508
SNP Nexus

SNPshotrs786205508
SNPdbers786205508
MSV3drs786205508
GWAS Ctlgrs786205508
Max Magnitude0
ClinVar
Risk rs786205508(T;T)
Alt rs786205508(T;T)
Reference rs786205508(C;C)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene MKS1
CLNDBN not provided
Reversed 1
HGVS NC_000017.10:g.56285903G>A
CLNSRC
CLNACC RCV000171263.1,