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rs796052929

From SNPedia

Orientationminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs796052929(G;G)
Make rs796052929(G;T)
ReferenceGRCh38.p2 38.2/146
Chromosome12
Position42468787
GenePRICKLE1
is asnp
is mentioned by
dbSNPrs796052929
ebirs796052929
HLIrs796052929
Exacrs796052929
Varsomers796052929
Maprs796052929
PheGenIrs796052929
hapmaprs796052929
1000 genomesrs796052929
hgdprs796052929
ensemblrs796052929
gopubmedrs796052929
geneviewrs796052929
scholarrs796052929
googlers796052929
pharmgkbrs796052929
gwascentralrs796052929
openSNPrs796052929
23andMers796052929
23andMe allrs796052929
SNP Nexus

SNPshotrs796052929
SNPdbers796052929
MSV3drs796052929
GWAS Ctlgrs796052929
Max Magnitude0
ClinVar
Risk rs796052929(G;G)
Alt rs796052929(G;G)
Reference rs796052929(T;T)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene PRICKLE1
CLNDBN not provided
Reversed 1
HGVS NC_000012.11:g.42862589A>C
CLNSRC
CLNACC RCV000188737.1,