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Variant : CV167198 (Single allele) Homo sapiens

Symbol: CV167198
Name: Single allele
Condition: Preeclampsia [RCV000161764]|Preeclampsia/eclampsia 1 [RCV000161764]
Clinical Significance: not provided
Last Evaluated:
Review Status: no assertion provided|not classified by submitter
Related Genes: ARHGAP11B   CHRFAM7A   GOLGA8H   GOLGA8J   GOLGA8Q   GOLGA8R   GOLGA8T   LINC02249  
Variant Type: deletion (SO:0000159)
Source: CLINVAR
Evidence: case-control
HGVS Name(s): NC_000015.10:g.30077711_30797323del
Position
Human AssemblyChrPosition (strand)Source
GRCh381530,077,711 - 30,797,323CLINVAR
GRCh371530,369,914 - 31,089,526CLINVAR
Cytogenetic Map1515q13.2CLINVAR
Trait Synonyms: Pre-eclampsia; Preeclampsia/eclampsia 1



References - uncurated

Additional Information

External Database Links
 
RGD Object Information
RGD ID: 9831982
Created: 2015-03-10
Species: Homo sapiens
Last Modified: 2019-10-08
Status: ACTIVE



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RGD is funded by grant HL64541 from the National Heart, Lung, and Blood Institute on behalf of the NIH.