Have questions? Visit https://www.reddit.com/r/SNPedia

rs63750194

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(AT;AT) 0 common in clinvar
(T;T) 0 common in clinvar
(TA;TA) 0 common in clinvar
Make rs63750194(-;-)
Make rs63750194(-;TA)
ReferenceGRCh38 38.1/141
Chromosome2
Position47804984
GeneMSH6
is asnp
is mentioned by
dbSNPrs63750194
ClinGenrs63750194
ebirs63750194
HLIrs63750194
Exacrs63750194
Varsomers63750194
Maprs63750194
PheGenIrs63750194
hapmaprs63750194
1000 genomesrs63750194
hgdprs63750194
ensemblrs63750194
gopubmedrs63750194
geneviewrs63750194
scholarrs63750194
googlers63750194
pharmgkbrs63750194
gwascentralrs63750194
openSNPrs63750194
23andMers63750194
23andMe allrs63750194
SNP Nexus

SNPshotrs63750194
SNPdbers63750194
MSV3drs63750194
GWAS Ctlgrs63750194
Max Magnitude0
ClinVar
Risk rs63750194(-;-)
Alt rs63750194(-;-)
Reference Rs63750194(AT;AT)
Significance Pathogenic
Disease Lynch syndrome Hereditary cancer-predisposing syndrome not provided
Variation info
Gene MSH6
CLNDBN Lynch syndrome Hereditary cancer-predisposing syndrome not provided
Reversed 0
HGVS NC_000002.11:g.48032123_48032124delTA
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000074871.2, RCV000162609.2, RCV000221153.1,