chr11:1853084:> Detail (hg38)

Information

Genome

Assembly Position
hg19 chr11:1,874,314-1,913,493 
hg38 chr11:1,853,084-1,892,263

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
0.242 ulcerative colitis NA CTD_human,GAD,GWASCAT Detail
0.120 heart valve disease NA CTD_human Detail
0.002 Inflammation NA GAD Detail
0.120 Inflammatory Bowel Diseases NA GWASCAT Detail
0.003 Lymphoma, Non-Hodgkin NA BeFree,GAD Detail
<0.001 melanoma NA BeFree Detail
<0.001 pneumonia Leukocyte-specific protein 1 regulates neutrophil recruitment in acute lung infl... BeFree 26320151 Detail
<0.001 Lymphoma, Large-Cell, Follicular NA BeFree Detail
<0.001 pancreatic carcinoma NA BeFree Detail
<0.001 Malignant neoplasm of lung NA BeFree Detail
<0.001 Adenocarcinoma of pancreas NA BeFree Detail
<0.001 Malignant neoplasm of pancreas NA BeFree Detail
<0.001 Carcinoma of lung NA BeFree Detail
0.120 Mammary Neoplasms NA CTD_human Detail
0.121 Mammographic Density NA BeFree,GWASCAT Detail
0.162 Malignant neoplasm of breast Confirmed BC risk SNPs rs17468277 (CASP8), rs1982073 (TGFB1), rs2981582 (FGFR2),... BeFree 22532573 Detail
0.004 breast carcinoma Confirmed BC risk SNPs rs17468277 (CASP8), rs1982073 (TGFB1), rs2981582 (FGFR2),... BeFree 22532573 Detail
<0.001 Astrocytoma NA BeFree Detail
0.120 Malignant neoplasm of urinary bladder NA GWASCAT Detail
0.120 calcinosis NA CTD_human Detail
Annotation

Annotations

DescrptionSourceLinks
NA DisGeNET Detail
NA DisGeNET Detail
NA DisGeNET Detail
NA DisGeNET Detail
NA DisGeNET Detail
NA DisGeNET Detail
Leukocyte-specific protein 1 regulates neutrophil recruitment in acute lung inflammation. DisGeNET Detail
NA DisGeNET Detail
NA DisGeNET Detail
NA DisGeNET Detail
NA DisGeNET Detail
NA DisGeNET Detail
NA DisGeNET Detail
NA DisGeNET Detail
NA DisGeNET Detail
Confirmed BC risk SNPs rs17468277 (CASP8), rs1982073 (TGFB1), rs2981582 (FGFR2), rs13281615 (8q24), ... DisGeNET Detail
Confirmed BC risk SNPs rs17468277 (CASP8), rs1982073 (TGFB1), rs2981582 (FGFR2), rs13281615 (8q24), ... DisGeNET Detail
NA DisGeNET Detail
NA DisGeNET Detail
NA DisGeNET Detail

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
rs1982073 dbSNP
Genome
hg38
Position
chr11:1,853,084-1,892,263
Variant Type
snv
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