Have questions? Visit https://www.reddit.com/r/SNPedia

rs786201007

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(-;-) 0 common in clinvar
Make rs786201007(-;AGGCGGAGCACCCCAAGCC)
Make rs786201007(AGGCGGAGCACCCCAAGCC;AGGCGGAGCACCCCAAGCC)
ReferenceGRCh38.p2 38.2/146
Chromosome12
Position12717916
GeneCDKN1B, GPR19
is asnp
is mentioned by
dbSNPrs786201007
dbSNP (old)rs786201007
ClinGenrs786201007
ebirs786201007
HLIrs786201007
Exacrs786201007
Varsomers786201007
Maprs786201007
PheGenIrs786201007
Biobankrs786201007
1000 genomesrs786201007
hgdprs786201007
ensemblrs786201007
gopubmedrs786201007
geneviewrs786201007
scholarrs786201007
googlers786201007
pharmgkbrs786201007
gwascentralrs786201007
openSNPrs786201007
23andMers786201007
23andMe allrs786201007
SNP Nexus

SNPshotrs786201007
SNPdbers786201007
MSV3drs786201007
GWAS Ctlgrs786201007
Max Magnitude0
ClinVar
Risk rs786201007(CAGGCGGAGCACCCCAAGC;CAGGCGGAGCACCCCAAGC)
Alt rs786201007(CAGGCGGAGCACCCCAAGC;CAGGCGGAGCACCCCAAGC)
Reference Rs786201007(-;-)
Significance Pathogenic
Disease Multiple endocrine neoplasia
Variation info
Gene LOC101929220 CDKN1B
CLNDBN Multiple endocrine neoplasia, type 4
Reversed 0
HGVS NC_000012.11:g.12870832_12870850dup19
CLNSRC OMIM Allelic Variant
CLNACC RCV000162205.4,