chr6:20534688:> Detail (hg19)

Information

Genome

Assembly Position
hg19 chr6:20,534,688-21,232,635
hg38 chr6:20,534,457-21,232,404 

HGVS

Type Transcript Protein
Summary

MGeND

Clinical significance
Variant entry
GWAS entry
Disease area statistics Show details

Frequency

[No Data.]

Prediction

[No Data.]

ClinVar

Clinical Significance
Review star [No Data.]
Show details
Links
Disease area statistics
[No Data.]
MGeND
[No Data.]
ClinVar
[No Data.]
CIViC
[No Data.]
DisGeNET
Score Disease name Description Source Pubmed Links
0.005 ulcerative colitis NA BeFree,GAD Detail
<0.001 colorectal carcinoma NA BeFree Detail
0.137 Crohn Disease NA GAD,GWASCAT Detail
0.005 Diabetes Mellitus, Insulin-Dependent NA GAD Detail
0.002 Fetal Diseases NA GAD Detail
0.002 HIV Infections NA GAD Detail
0.002 hyperglycemia NA GAD Detail
0.125 Inflammatory Bowel Diseases NA GAD,GWASCAT Detail
0.005 Insulin resistance NA GAD Detail
<0.001 insulinoma NA BeFree Detail
0.008 obesity NA BeFree,GAD Detail
<0.001 Ovarian Diseases NA BeFree Detail
0.007 psoriasis NA BeFree,GAD Detail
0.002 Rectal Fistula NA GAD Detail
0.002 Starvation NA GAD Detail
0.002 Tobacco use disorder NA GAD Detail
0.123 gestational diabetes NA BeFree,GAD,GWASCAT Detail
0.002 Malnutrition NA GAD Detail
<0.001 Impaired glucose tolerance NA BeFree Detail
0.003 Metabolic syndrome X NA BeFree,GAD Detail
<0.001 Carcinoma of bladder NA BeFree Detail
<0.001 colorectal cancer NA BeFree Detail
0.003 coronary artery disease NA BeFree,GAD Detail
0.002 Spontaneous abortion NA GAD Detail
0.002 Albuminuria NA GAD Detail
0.123 gestational diabetes The minor alleles of rs7903146 (TCF7L2), rs12255372 (TCF7L2), rs1799884 (-30G/A,... BeFree 23690305 Detail
<0.001 arteriosclerosis NA BeFree Detail
0.005 atherosclerosis NA BeFree,GAD Detail
0.120 Birth Weight NA CTD_human Detail
0.120 Malignant neoplasm of urinary bladder NA BeFree,GWASCAT Detail
0.120 Body Weight NA CTD_human Detail
0.002 calcinosis NA GAD Detail
Annotation

Overlapped Transcript Coordinates

Gene Transcript ID Exon Number Chromosome Start Stop Type Amino Mutation Transcript Position Links

Overlapped Transcript

Gene Transcript ID Chromosome Start Stop Links
Gene
-
dbSNP
rs386597997 dbSNP
Genome
hg19
Position
chr6:20,534,688-21,232,635
Variant Type
snv
Genome browser