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rs1060500186

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(GGAC;GGAC) 0 common in clinvar
Make rs1060500186(-;-)
Make rs1060500186(-;GACG)
Make rs1060500186(GACG;GACG)
ReferenceGRCh38.p7 38.3/150
Chromosome12
Position12717888
GeneCDKN1B, GPR19
is asnp
is mentioned by
dbSNPrs1060500186
dbSNP (classic)rs1060500186
ClinGenrs1060500186
ebirs1060500186
HLIrs1060500186
Exacrs1060500186
Gnomadrs1060500186
Varsomers1060500186
LitVarrs1060500186
Maprs1060500186
PheGenIrs1060500186
Biobankrs1060500186
1000 genomesrs1060500186
hgdprs1060500186
ensemblrs1060500186
geneviewrs1060500186
scholarrs1060500186
googlers1060500186
pharmgkbrs1060500186
gwascentralrs1060500186
openSNPrs1060500186
23andMers1060500186
23andMe allrs1060500186
SNPshotrs1060500186
SNPdbers1060500186
MSV3drs1060500186
GWAS Ctlgrs1060500186
Max Magnitude0
ClinVar
Risk rs1060500186(-;-)
Alt rs1060500186(-;-)
Reference Rs1060500186(GGAC;GGAC)
Significance Pathogenic
Disease Multiple endocrine neoplasia
Variation info
Gene CDKN1B
CLNDBN Multiple endocrine neoplasia, type 4
Reversed 0
HGVS NC_000012.11:g.12870822_12870825delGACG
CLNSRC
CLNACC RCV000464377.1,