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rs587777698

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs587777698(C;T)
Make rs587777698(T;T)
ReferenceGRCh38 38.1/142
Chromosome12
Position6944607
GeneC12orf57, PTPN6
is asnp
is mentioned by
dbSNPrs587777698
ClinGenrs587777698
ebirs587777698
HLIrs587777698
Exacrs587777698
Varsomers587777698
Maprs587777698
PheGenIrs587777698
hapmaprs587777698
1000 genomesrs587777698
hgdprs587777698
ensemblrs587777698
gopubmedrs587777698
geneviewrs587777698
scholarrs587777698
googlers587777698
pharmgkbrs587777698
gwascentralrs587777698
openSNPrs587777698
23andMers587777698
23andMe allrs587777698
SNP Nexus

SNPshotrs587777698
SNPdbers587777698
MSV3drs587777698
GWAS Ctlgrs587777698
Max Magnitude0
ClinVar
Risk rs587777698(T;T)
Alt rs587777698(T;T)
Reference Rs587777698(C;C)
Significance Pathogenic
Disease Temtamy syndrome not provided
Variation info
Gene C12orf57 PTPN6
CLNDBN Temtamy syndrome not provided
Reversed 0
HGVS NC_000012.11:g.7053770C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000143978.2, RCV000414658.1,