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rs786205258

From SNPedia

Orientationplus
Geno Mag Summary
(TT;TT) 0 common in clinvar
Make rs786205258(-;-)
Make rs786205258(-;TT)
ReferenceGRCh38.p2 38.2/146
Chromosome16
Position46692443
GeneORC6
is asnp
is mentioned by
dbSNPrs786205258
ebirs786205258
HLIrs786205258
Exacrs786205258
Varsomers786205258
Maprs786205258
PheGenIrs786205258
hapmaprs786205258
1000 genomesrs786205258
hgdprs786205258
ensemblrs786205258
gopubmedrs786205258
geneviewrs786205258
scholarrs786205258
googlers786205258
pharmgkbrs786205258
gwascentralrs786205258
openSNPrs786205258
23andMers786205258
23andMe allrs786205258
SNP Nexus

SNPshotrs786205258
SNPdbers786205258
MSV3drs786205258
GWAS Ctlgrs786205258
Max Magnitude0
ClinVar
Risk rs786205258(;)
Alt rs786205258(;)
Reference rs786205258(TT;TT)
Significance Pathogenic
Disease Meier-Gorlin syndrome 3
Variation info
Gene ORC6
CLNDBN Meier-Gorlin syndrome 3
Reversed 0
HGVS NC_000016.9:g.46726355_46726356delTT
CLNSRC OMIM Allelic Variant
CLNACC RCV000023632.5,