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rs869312166

From SNPedia

Orientationplus
Geno Mag Summary
(GAGA;GAGA) 0 common in clinvar
Make rs869312166(-;-)
Make rs869312166(-;AGAG)
Make rs869312166(AGAG;AGAG)
ReferenceGRCh38.p2 38.2/147
Chromosome12
Position12717811
GeneCDKN1B, GPR19
is asnp
is mentioned by
dbSNPrs869312166
ebirs869312166
HLIrs869312166
Exacrs869312166
Varsomers869312166
Maprs869312166
PheGenIrs869312166
hapmaprs869312166
1000 genomesrs869312166
hgdprs869312166
ensemblrs869312166
gopubmedrs869312166
geneviewrs869312166
scholarrs869312166
googlers869312166
pharmgkbrs869312166
gwascentralrs869312166
openSNPrs869312166
23andMers869312166
23andMe allrs869312166
SNP Nexus

SNPshotrs869312166
SNPdbers869312166
MSV3drs869312166
GWAS Ctlgrs869312166
Max Magnitude0
ClinVar
Risk rs869312166(;)
Alt rs869312166(;)
Reference rs869312166(GAGA;GAGA)
Significance Pathogenic
Disease Multiple endocrine neoplasia Primary hyperparathyroidism
Variation info
Gene LOC101929220 CDKN1B
CLNDBN Multiple endocrine neoplasia, type 4 Primary hyperparathyroidism
Reversed 0
HGVS NC_000012.11:g.12870745_12870748delAGAG
CLNSRC OMIM Allelic Variant
CLNACC RCV000162206.3, RCV000210358.1,