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

rs730881758

From SNPedia

Orientationplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs730881758(A;T)
Make rs730881758(T;T)
ReferenceGRCh38.p2 38.2/144
Chromosome2
Position47466672
GeneMSH2
is asnp
is mentioned by
dbSNPrs730881758
ebirs730881758
HLIrs730881758
Exacrs730881758
Varsomers730881758
Maprs730881758
PheGenIrs730881758
hapmaprs730881758
1000 genomesrs730881758
hgdprs730881758
ensemblrs730881758
gopubmedrs730881758
geneviewrs730881758
scholarrs730881758
googlers730881758
pharmgkbrs730881758
gwascentralrs730881758
openSNPrs730881758
23andMers730881758
23andMe allrs730881758
SNP Nexus

SNPshotrs730881758
SNPdbers730881758
MSV3drs730881758
GWAS Ctlgrs730881758
Max Magnitude0
ClinVar
Risk rs730881758(T;T)
Alt rs730881758(T;T)
Reference rs730881758(A;A)
Significance Pathogenic
Disease not provided
Variation info
Gene MSH2
CLNDBN not provided
Reversed 0
HGVS NC_000002.11:g.47693811A>T
CLNSRC
CLNACC RCV000160590.1,