Rs1801133
id:
rs1801133-307-16721134
title:
Rs1801133
text:
C677T or rs1801133 is a genetic variation—a single nucleotide polymorphism (SNP)—in the MTHFR gene. Among Americans the frequency of T-homozygosity ranges from 1% or less among people of sub-Saharan African descent to 20% or more among Italians and Hispanics. It has been related to schizophrenia
Alzheimer's disease
depression
autism
spina bifida. In 2000 association studies on oral clefts, Down syndrome, and fetal anticonvulsant syndrome were either unreplicated or had yielded conflicting result
brand slug:
wiki
category slug:
encyclopedia
description:
Single Nucleotide Polymorphism within the MTHFR gene
original url:
https://en.wikipedia.org/wiki/Rs1801133
date created:
date modified:
2023-08-24T08:39:11Z
main entity:
{"identifier":"Q4048578","url":"https://www.wikidata.org/entity/Q4048578"}
image:
fields total:
13
integrity:
14