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

rs730881734

From SNPedia

Orientationplus
Geno Mag Summary
(AGAAAGA;AGAAAGA) 0 common in clinvar
Make rs730881734(-;-)
Make rs730881734(-;AAGAAGA)
Make rs730881734(AAGAAGA;AAGAAGA)
ReferenceGRCh38.p2 38.2/144
Chromosome3
Position37000956
GeneMLH1
is asnp
is mentioned by
dbSNPrs730881734
ebirs730881734
HLIrs730881734
Exacrs730881734
Varsomers730881734
Maprs730881734
PheGenIrs730881734
hapmaprs730881734
1000 genomesrs730881734
hgdprs730881734
ensemblrs730881734
gopubmedrs730881734
geneviewrs730881734
scholarrs730881734
googlers730881734
pharmgkbrs730881734
gwascentralrs730881734
openSNPrs730881734
23andMers730881734
23andMe allrs730881734
SNP Nexus

SNPshotrs730881734
SNPdbers730881734
MSV3drs730881734
GWAS Ctlgrs730881734
Max Magnitude0
ClinVar
Risk rs730881734(;)
Alt rs730881734(;)
Reference rs730881734(AGAAAGA;AGAAAGA)
Significance Pathogenic
Disease Hereditary cancer-predisposing syndrome
Variation info
Gene MLH1
CLNDBN Hereditary cancer-predisposing syndrome
Reversed 0
HGVS NC_000003.11:g.37042447_37042453delAAGAAGA
CLNSRC
CLNACC RCV000160516.1,