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rs863225379

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(GTTGAGTTTCTGAA;GTTGAGTTTCTGAA) 0 common in clinvar
Make rs863225379(GTTGAGTTTCTGAA;T)
Make rs863225379(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome3
Position37047621
GeneMLH1
is asnp
is mentioned by
dbSNPrs863225379
dbSNP (old)rs863225379
ClinGenrs863225379
ebirs863225379
HLIrs863225379
Exacrs863225379
Gnomadrs863225379
Varsomers863225379
Maprs863225379
PheGenIrs863225379
Biobankrs863225379
1000 genomesrs863225379
hgdprs863225379
ensemblrs863225379
gopubmedrs863225379
geneviewrs863225379
scholarrs863225379
googlers863225379
pharmgkbrs863225379
gwascentralrs863225379
openSNPrs863225379
23andMers863225379
23andMe allrs863225379
SNP Nexus

SNPshotrs863225379
SNPdbers863225379
MSV3drs863225379
GWAS Ctlgrs863225379
Max Magnitude0
ClinVar
Risk rs863225379(T;T)
Alt rs863225379(T;T)
Reference Rs863225379(GTTGAGTTTCTGAA;GTTGAGTTTCTGAA)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene MLH1
CLNDBN not provided
Reversed 0
HGVS NC_000003.11:g.37089112_37089125delGTTGAGTTTCTGAAinsT
CLNSRC
CLNACC RCV000202082.1,