chr10:16257952:C>T Detail (hg38)

Information

Genome

Assembly Position
hg19 chr10:16,299,951-16,299,951 View the variant detail on this assembly version.
hg38 chr10:16,257,952-16,257,952

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
0.006 obesity [In addition to FTO and MC4R, we detected significant association of obesity wit... GAD 19151714 Detail
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
0.002 obesity [Genome-wide association study for early-onset and morbid adult obesity identifi... GAD 19151714 Detail
Annotation

Annotations

DescrptionSourceLinks
[In addition to FTO and MC4R, we detected significant association of obesity with three new risk loc... DisGeNET Detail
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
[Genome-wide association study for early-onset and morbid adult obesity identifies three new risk lo... DisGeNET Detail
Gene
-
dbSNP
rs10508503 dbSNP
Genome
hg38
Position
chr10:16,257,952-16,257,952
Variant Type
snv
Reference Allele
C
Alternative Allele
T
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