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rs774454456

From SNPedia

Orientationplus
Geno Mag Summary
(GAGA;GAGA) 0 common in clinvar
Make rs774454456(-;-)
Make rs774454456(-;GAGA)
ReferenceGRCh38.p2 38.2/144
Chromosome12
Position12717808
GeneCDKN1B, GPR19
is asnp
is mentioned by
dbSNPrs774454456
ebirs774454456
HLIrs774454456
Exacrs774454456
Varsomers774454456
Maprs774454456
PheGenIrs774454456
hapmaprs774454456
1000 genomesrs774454456
hgdprs774454456
ensemblrs774454456
gopubmedrs774454456
geneviewrs774454456
scholarrs774454456
googlers774454456
pharmgkbrs774454456
gwascentralrs774454456
openSNPrs774454456
23andMers774454456
23andMe allrs774454456
SNP Nexus

SNPshotrs774454456
SNPdbers774454456
MSV3drs774454456
GWAS Ctlgrs774454456
Max Magnitude0
ClinVar
Risk rs774454456(;)
Alt rs774454456(;)
Reference rs774454456(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,