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rs777354267

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs777354267(C;T)
Make rs777354267(T;T)
ReferenceGRCh38.p2 38.2/144
Chromosome12
Position12718045
GeneCDKN1B, GPR19
is asnp
is mentioned by
dbSNPrs777354267
ebirs777354267
HLIrs777354267
Exacrs777354267
Varsomers777354267
Maprs777354267
PheGenIrs777354267
hapmaprs777354267
1000 genomesrs777354267
hgdprs777354267
ensemblrs777354267
gopubmedrs777354267
geneviewrs777354267
scholarrs777354267
googlers777354267
pharmgkbrs777354267
gwascentralrs777354267
openSNPrs777354267
23andMers777354267
23andMe allrs777354267
SNP Nexus

SNPshotrs777354267
SNPdbers777354267
MSV3drs777354267
GWAS Ctlgrs777354267
Max Magnitude0
ClinVar
Risk rs777354267(T;T)
Alt rs777354267(T;T)
Reference rs777354267(C;C)
Significance Pathogenic
Disease Multiple endocrine neoplasia
Variation info
Gene LOC101929220 CDKN1B
CLNDBN Multiple endocrine neoplasia, type 4
Reversed 0
HGVS NC_000012.11:g.12870979C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000162207.3,