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rs756853299

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs756853299(A;A)
Make rs756853299(A;G)
ReferenceGRCh38.p2 38.2/147
Chromosome17
Position58214748
GeneMKS1
is asnp
is mentioned by
dbSNPrs756853299
ebirs756853299
HLIrs756853299
Exacrs756853299
Varsomers756853299
Maprs756853299
PheGenIrs756853299
hapmaprs756853299
1000 genomesrs756853299
hgdprs756853299
ensemblrs756853299
gopubmedrs756853299
geneviewrs756853299
scholarrs756853299
googlers756853299
pharmgkbrs756853299
gwascentralrs756853299
openSNPrs756853299
23andMers756853299
23andMe allrs756853299
SNP Nexus

SNPshotrs756853299
SNPdbers756853299
MSV3drs756853299
GWAS Ctlgrs756853299
Max Magnitude0
ClinVar
Risk rs756853299(A;A)
Alt rs756853299(A;A)
Reference rs756853299(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene MKS1
CLNDBN not provided
Reversed 0
HGVS NC_000017.10:g.56292109G>A
CLNSRC
CLNACC RCV000224251.1,