MLH3, mutL homolog 3, 27030

N. diseases: 108; N. variants: 18
Source: ALL
Variant DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Disease Disease Class Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs587776622
rs587776622
1.000 0.080 14 75047174 stop gained C/A snv 7.0E-06
CUI: C0009402
Disease: Colorectal Carcinoma
Colorectal Carcinoma
Digestive System Diseases; Neoplasms 0.700 0
dbSNP: rs108621
rs108621
1.000 0.080 14 75013934 3 prime UTR variant T/C snv 0.43
CUI: C0009402
Disease: Colorectal Carcinoma
Colorectal Carcinoma
Digestive System Diseases; Neoplasms 0.010 1.000 1 2018 2018
dbSNP: rs175080
rs175080
0.776 0.240 14 75047125 missense variant G/A snv 0.40 0.43
CUI: C0009402
Disease: Colorectal Carcinoma
Colorectal Carcinoma
Digestive System Diseases; Neoplasms 0.010 < 0.001 1 2004 2004
dbSNP: rs28756992
rs28756992
0.925 0.080 14 75047123 missense variant T/C snv 1.1E-02 1.5E-02
CUI: C0009402
Disease: Colorectal Carcinoma
Colorectal Carcinoma
Digestive System Diseases; Neoplasms 0.010 < 0.001 1 2004 2004