chr5:135226137:C>T Detail (hg19)

Information

Genome

Assembly Position
hg19 chr5:135,226,137-135,226,137
hg38 chr5:135,890,448-135,890,448 View the variant detail on this assembly version.

HGVS

[No Data.]
Summary

MGeND

Clinical significance
Variant entry
GWAS entry
Disease area statistics Show details

Frequency

[No Data.]

Prediction

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
<0.001 Childhood asthma IL9 polymorphisms (rs11741137, rs2069885, and rs1859430) showed evidence for int... BeFree 25913104 Detail
Annotation

Annotations

DescrptionSourceLinks
IL9 polymorphisms (rs11741137, rs2069885, and rs1859430) showed evidence for interaction with dust m... DisGeNET Detail
Gene
-
dbSNP
rs11741137 dbSNP
Genome
hg19
Position
chr5:135,226,137-135,226,137
Variant Type
snv
Reference Allele
C
Alternative Allele
T
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