Bibliome.ai browser hg19
Search
About
Stats
FAQ
KCNQ1 c.1514+52872A>G
Variant ID: 11-2736183-A-G
NM_000218.2(
KCNQ1
):c.1514+52872A>G
This variant was identified in 1 publication
View GRCh38 version.
Variant-Specific Resource Links:
gnomAD v2.1.1
Mutalizer Name Checker
Google
UCSC Genome Browser
ClinVar
dbSNP
Publications:
Human imprinted chromosomal regions are historical hot-spots of recombination.
Plos Genetics
Sandovici, Ionel I; Kassovska-Bratinova, Sacha S; Vaughan, Joe E JE; Stewart, Rae R; Leppert, Mark M; Sapienza, Carmen C
Publication Date: 2006-07
Variant appearance in text: rs231847
PubMed Link:
16839189
Variant Present in the following documents:
Main text
pgen.0020101.pdf
View BVdb publication page