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rs863223312

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(GTAAATCA;GTAAATCA) 0 common in clinvar
Make rs863223312(ATTT;ATTT)
Make rs863223312(ATTT;GTAAATCA)
ReferenceGRCh38.p2 38.2/146
Chromosome3
Position37040295
GeneMLH1
is asnp
is mentioned by
dbSNPrs863223312
dbSNP (old)rs863223312
ClinGenrs863223312
ebirs863223312
HLIrs863223312
Exacrs863223312
Gnomadrs863223312
Varsomers863223312
Maprs863223312
PheGenIrs863223312
Biobankrs863223312
1000 genomesrs863223312
hgdprs863223312
ensemblrs863223312
gopubmedrs863223312
geneviewrs863223312
scholarrs863223312
googlers863223312
pharmgkbrs863223312
gwascentralrs863223312
openSNPrs863223312
23andMers863223312
23andMe allrs863223312
SNP Nexus

SNPshotrs863223312
SNPdbers863223312
MSV3drs863223312
GWAS Ctlgrs863223312
Max Magnitude0
ClinVar
Risk rs863223312(ATTT;ATTT)
Alt rs863223312(ATTT;ATTT)
Reference Rs863223312(GTAAATCA;GTAAATCA)
Significance Pathogenic
Disease Lynch syndrome II
Variation info
Gene MLH1
CLNDBN Lynch syndrome II
Reversed 0
HGVS NC_000003.11:g.37081786_37081793delGTAAATCAinsATTT
CLNSRC OMIM Allelic Variant
CLNACC RCV000018613.27,