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rs786204104

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs786204104(-;-)
Make rs786204104(-;C)
ReferenceGRCh38.p2 38.2/146
Chromosome7
Position5987580
GenePMS2
is asnp
is mentioned by
dbSNPrs786204104
ebirs786204104
HLIrs786204104
Exacrs786204104
Varsomers786204104
Maprs786204104
PheGenIrs786204104
hapmaprs786204104
1000 genomesrs786204104
hgdprs786204104
ensemblrs786204104
gopubmedrs786204104
geneviewrs786204104
scholarrs786204104
googlers786204104
pharmgkbrs786204104
gwascentralrs786204104
openSNPrs786204104
23andMers786204104
23andMe allrs786204104
SNP Nexus

SNPshotrs786204104
SNPdbers786204104
MSV3drs786204104
GWAS Ctlgrs786204104
Max Magnitude0
ClinVar
Risk rs786204104(;)
Alt rs786204104(;)
Reference rs786204104(C;C)
Significance Pathogenic
Disease Lynch syndrome
Variation info
Gene PMS2
CLNDBN Lynch syndrome
Reversed 1
HGVS NC_000007.13:g.6027211delG
CLNSRC
CLNACC RCV000168035.1,