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rs748863662

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;T) 3 Carrier of an autosomal recessive polycystic kidney disease mutation
(T;T) 0 common/normal


Make rs748863662(C;C)
ReferenceGRCh38.p2 38.2/147
Chromosome6
Position51659724
GeneLOC105375087, PKHD1
is asnp
is mentioned by
dbSNPrs748863662
dbSNP (old)rs748863662
ClinGenrs748863662
ebirs748863662
HLIrs748863662
Exacrs748863662
Gnomadrs748863662
Varsomers748863662
Maprs748863662
PheGenIrs748863662
Biobankrs748863662
1000 genomesrs748863662
hgdprs748863662
ensemblrs748863662
gopubmedrs748863662
geneviewrs748863662
scholarrs748863662
googlers748863662
pharmgkbrs748863662
gwascentralrs748863662
openSNPrs748863662
23andMers748863662
23andMe allrs748863662
SNP Nexus

SNPshotrs748863662
SNPdbers748863662
MSV3drs748863662
GWAS Ctlgrs748863662
Max Magnitude3