chr6:22078615:G>A Detail (hg19)

Information

Genome

Assembly Position
hg19 chr6:22,078,615-22,078,615
hg38 chr6:22,078,386-22,078,386 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

JP HGVD:[No Data.]
ToMMo:0.835
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
0.005 obesity In each study, we tested associations of rs4712652 (near-PRL), rs10508503 (near-... BeFree 22430306 Detail
<0.001 Overweight In each study, we tested associations of rs4712652 (near-PRL), rs10508503 (near-... BeFree 22430306 Detail
0.005 obesity A common variant (rs4712652) adjacent to the prolactin gene was recently associa... BeFree 20846890 Detail
Annotation

Annotations

DescrptionSourceLinks
In each study, we tested associations of rs4712652 (near-PRL), rs10508503 (near-PTER), rs1424233 (ne... DisGeNET Detail
In each study, we tested associations of rs4712652 (near-PRL), rs10508503 (near-PTER), rs1424233 (ne... DisGeNET Detail
A common variant (rs4712652) adjacent to the prolactin gene was recently associated with obesity usi... DisGeNET Detail
Gene
-
dbSNP
rs4712652 dbSNP
Genome
hg19
Position
chr6:22,078,615-22,078,615
Variant Type
snv
Reference Allele
G
Alternative Allele
A
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))
rs4712652
Allele frequency, for each ALT allele (ToMMo 8.3KJPN Allele Frequency Panel(v20200831))
0.8348
Allele count in genotypes, for each ALT allele (ToMMo 8.3KJPN Allele Frequency Panel(v20200831))
13991
Total number of alleles in called genotypes (ToMMo 8.3KJPN Allele Frequency Panel(v20200831))
16760
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