chr10:129233875:C>G Detail (hg38)

Information

Genome

Assembly Position
hg19 chr10:131,032,139-131,032,139 View the variant detail on this assembly version.
hg38 chr10:129,233,875-129,233,875

HGVS

[No Data.]
Summary

MGeND

Clinical significance
Variant entry
GWAS entry
Disease area statistics Show details

Frequency

JP HGVD:[No Data.]
ToMMo:1.000
NCBN:[No Data.]
NCBN(Hondo):[No Data.]
NCBN(Ryukyu):[No Data.]
East asia ExAC:[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
0.154 asthma These results suggest that the SNPs in IL-12A rs568404 and IL-12B rs3212227 may ... BeFree 21513752 Detail
Annotation

Annotations

DescrptionSourceLinks
These results suggest that the SNPs in IL-12A rs568404 and IL-12B rs3212227 may individually and joi... DisGeNET Detail
Gene
-
dbSNP
rs568404 dbSNP
Genome
hg38
Position
chr10:129,233,875-129,233,875
Variant Type
snv
Reference Allele
C
Alternative Allele
G
ToMMo VCF FILTER column value (ToMMo 8.3KJPN Allele Frequency Panel(v20200831))
PASS
Total VCF ID column value (ToMMo 8.3KJPN Allele Frequency Panel(v20200831))
rs568404
Allele frequency, for each ALT allele (ToMMo 8.3KJPN Allele Frequency Panel(v20200831))
1
Allele count in genotypes, for each ALT allele (ToMMo 8.3KJPN Allele Frequency Panel(v20200831))
16760
Total number of alleles in called genotypes (ToMMo 8.3KJPN Allele Frequency Panel(v20200831))
16760
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