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rs41542214

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs41542214(A;A)
Make rs41542214(A;C)
ReferenceGRCh38.p2 38.2/144
Chromosome3
Position37048979
GeneMLH1
is asnp
is mentioned by
dbSNPrs41542214
ebirs41542214
HLIrs41542214
Exacrs41542214
Varsomers41542214
Maprs41542214
PheGenIrs41542214
hapmaprs41542214
1000 genomesrs41542214
hgdprs41542214
ensemblrs41542214
gopubmedrs41542214
geneviewrs41542214
scholarrs41542214
googlers41542214
pharmgkbrs41542214
gwascentralrs41542214
openSNPrs41542214
23andMers41542214
23andMe allrs41542214
SNP Nexus

SNPshotrs41542214
SNPdbers41542214
MSV3drs41542214
GWAS Ctlgrs41542214
Max Magnitude0
ClinVar
Risk rs41542214(A,T;A,T)
Alt rs41542214(A,T;A,T)
Reference rs41542214(C;C)
Significance Pathogenic
Disease Tumor susceptibility linked to germline BAP1 mutations not provided
Variation info
Gene MLH1
CLNDBN Tumor susceptibility linked to germline BAP1 mutations not provided
Reversed 0
HGVS NC_000003.11:g.37090470C>A; NC_000003.11:g.37090470C>T
CLNSRC
CLNACC RCV000221202.1, RCV000160542.1,