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rs786201010

From SNPedia

Orientationplus
Geno Mag Summary
(CCTT;CCTT) 0 common in clinvar
Make rs786201010(-;-)
Make rs786201010(-;CCTT)
ReferenceGRCh38.p2 38.2/146
Chromosome12
Position12717384
GeneCDKN1B, GPR19
is asnp
is mentioned by
dbSNPrs786201010
ebirs786201010
HLIrs786201010
Exacrs786201010
Varsomers786201010
Maprs786201010
PheGenIrs786201010
hapmaprs786201010
1000 genomesrs786201010
hgdprs786201010
ensemblrs786201010
gopubmedrs786201010
geneviewrs786201010
scholarrs786201010
googlers786201010
pharmgkbrs786201010
gwascentralrs786201010
openSNPrs786201010
23andMers786201010
23andMe allrs786201010
SNP Nexus

SNPshotrs786201010
SNPdbers786201010
MSV3drs786201010
GWAS Ctlgrs786201010
Max Magnitude0
ClinVar
Risk rs786201010(;)
Alt rs786201010(;)
Reference rs786201010(CCTT;CCTT)
Significance Pathogenic
Disease Multiple endocrine neoplasia
Variation info
Gene LOC101929220 CDKN1B
CLNDBN Multiple endocrine neoplasia, type 4
Reversed 0
HGVS NC_000012.11:g.12870318_12870321delCCTT
CLNSRC OMIM Allelic Variant
CLNACC RCV000162208.3,