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rs533778281

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs533778281(C;C)
Make rs533778281(C;G)
ReferenceGRCh38.p2 38.2/144
Chromosome22
Position38016774
GeneLOC105373026, POLR2F
is asnp
is mentioned by
dbSNPrs533778281
ebirs533778281
HLIrs533778281
Exacrs533778281
Varsomers533778281
Maprs533778281
PheGenIrs533778281
hapmaprs533778281
1000 genomesrs533778281
hgdprs533778281
ensemblrs533778281
gopubmedrs533778281
geneviewrs533778281
scholarrs533778281
googlers533778281
pharmgkbrs533778281
gwascentralrs533778281
openSNPrs533778281
23andMers533778281
23andMe allrs533778281
SNP Nexus

SNPshotrs533778281
SNPdbers533778281
MSV3drs533778281
GWAS Ctlgrs533778281
Merged fromRs606231341
Max Magnitude0
ClinVar
Risk rs533778281(C;C)
Alt rs533778281(C;C)
Reference rs533778281(G;G)
Significance Probable-Pathogenic
Disease Hirschsprung disease 1
Variation info
Gene LOC101927099 POLR2F
CLNDBN Hirschsprung disease 1
Reversed 0
HGVS NC_000022.10:g.38412781G>C
CLNSRC
CLNACC RCV000144843.1,