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rs267608159

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(AAA;AAA) 0 common in clinvar
Make rs267608159(-;-)
Make rs267608159(-;AAA)
ReferenceGRCh38.p7 38.3/149
Chromosome7
Position5987526
GenePMS2
is asnp
is mentioned by
dbSNPrs267608159
dbSNP (classic)rs267608159
ClinGenrs267608159
ebirs267608159
HLIrs267608159
Exacrs267608159
Gnomadrs267608159
Varsomers267608159
LitVarrs267608159
Maprs267608159
PheGenIrs267608159
Biobankrs267608159
1000 genomesrs267608159
hgdprs267608159
ensemblrs267608159
geneviewrs267608159
scholarrs267608159
googlers267608159
pharmgkbrs267608159
gwascentralrs267608159
openSNPrs267608159
23andMers267608159
23andMe allrs267608159
SNPshotrs267608159
SNPdbers267608159
MSV3drs267608159
GWAS Ctlgrs267608159
Max Magnitude0
ClinVar
Risk rs267608159(-;-)
Alt rs267608159(-;-)
Reference Rs267608159(AAA;AAA)
Significance Pathogenic
Disease Hereditary nonpolyposis colorectal cancer type 4 Lynch syndrome
Variation info
Gene PMS2
CLNDBN Hereditary nonpolyposis colorectal cancer type 4 Lynch syndrome
Reversed 1
HGVS NC_000007.13:g.6027157_6027159delTTT
CLNSRC OMIM Allelic Variant PMS2 @ LOVD
CLNACC RCV000009820.4, RCV000076803.2,