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rs786201011

From SNPedia

Orientationplus
Geno Mag Summary
(CT;CT) 0 common in clinvar
Make rs786201011(-;-)
Make rs786201011(-;CT)
ReferenceGRCh38.p2 38.2/146
Chromosome12
Position12718213
GeneCDKN1B, GPR19
is asnp
is mentioned by
dbSNPrs786201011
ebirs786201011
HLIrs786201011
Exacrs786201011
Varsomers786201011
Maprs786201011
PheGenIrs786201011
hapmaprs786201011
1000 genomesrs786201011
hgdprs786201011
ensemblrs786201011
gopubmedrs786201011
geneviewrs786201011
scholarrs786201011
googlers786201011
pharmgkbrs786201011
gwascentralrs786201011
openSNPrs786201011
23andMers786201011
23andMe allrs786201011
SNP Nexus

SNPshotrs786201011
SNPdbers786201011
MSV3drs786201011
GWAS Ctlgrs786201011
Max Magnitude0
ClinVar
Risk rs786201011(;)
Alt rs786201011(;)
Reference rs786201011(CT;CT)
Significance Pathogenic
Disease Multiple endocrine neoplasia
Variation info
Gene LOC101929220 CDKN1B
CLNDBN Multiple endocrine neoplasia, type 4
Reversed 0
HGVS NC_000012.11:g.12871147_12871148delCT
CLNSRC OMIM Allelic Variant
CLNACC RCV000162209.3,