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rs786201014

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs786201014(A;A)
Make rs786201014(A;G)
ReferenceGRCh38.p2 38.2/146
Chromosome18
Position32042196
GeneRNF125
is asnp
is mentioned by
dbSNPrs786201014
ebirs786201014
HLIrs786201014
Exacrs786201014
Varsomers786201014
Maprs786201014
PheGenIrs786201014
hapmaprs786201014
1000 genomesrs786201014
hgdprs786201014
ensemblrs786201014
gopubmedrs786201014
geneviewrs786201014
scholarrs786201014
googlers786201014
pharmgkbrs786201014
gwascentralrs786201014
openSNPrs786201014
23andMers786201014
23andMe allrs786201014
SNP Nexus

SNPshotrs786201014
SNPdbers786201014
MSV3drs786201014
GWAS Ctlgrs786201014
Max Magnitude0
ClinVar
Risk rs786201014(A;A)
Alt rs786201014(A;A)
Reference rs786201014(G;G)
Significance Pathogenic
Disease Tenorio syndrome
Variation info
Gene RNF125
CLNDBN Tenorio syndrome
Reversed 0
HGVS NC_000018.9:g.29622159G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000162241.3,