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rs797044902

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs797044902(C;T)
Make rs797044902(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome16
Position2106248
GeneMIR6511B1, PKD1
is asnp
is mentioned by
dbSNPrs797044902
ebirs797044902
HLIrs797044902
Exacrs797044902
Varsomers797044902
Maprs797044902
PheGenIrs797044902
hapmaprs797044902
1000 genomesrs797044902
hgdprs797044902
ensemblrs797044902
gopubmedrs797044902
geneviewrs797044902
scholarrs797044902
googlers797044902
pharmgkbrs797044902
gwascentralrs797044902
openSNPrs797044902
23andMers797044902
23andMe allrs797044902
SNP Nexus

SNPshotrs797044902
SNPdbers797044902
MSV3drs797044902
GWAS Ctlgrs797044902
Max Magnitude0
ClinVar
Risk rs797044902(T;T)
Alt rs797044902(T;T)
Reference rs797044902(C;C)
Significance Probable-Pathogenic
Disease Inborn genetic diseases
Variation info
Gene MIR6511B1 PKD1
CLNDBN Inborn genetic diseases
Reversed 1
HGVS NC_000016.9:g.2156249G>A
CLNSRC
CLNACC RCV000190727.1,